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BOC-HYP(BZL)-OH

CAS No.
54631-81-1
Chemical Name:
BOC-HYP(BZL)-OH
Synonyms
BOC-HYP(BZL);BOC-HYP(BZL)-OH;BOC-L-HYP(BZL)-OH;Boc-Hyp(Bzl)·DCHA;BOC-PRO(4-OBZL)-OH;BOC-HYP(BZL)-OH DCHA;Boc-L-Hyp(Bzl)-OH·DCHA;BOC-HYP(BZL)-OH·DCHA,98%;BOC-HYP(BZL)-OH USP/EP/BP;BOC-HYDROXYPROLINE(BZL)-OH
CBNumber:
CB6148544
Molecular Formula:
C17H23NO5
Molecular Weight:
321.37
MDL Number:
MFCD00037325
MOL File:
54631-81-1.mol
Last updated:2026-01-13 11:25:41
Product description Number Pack Size Price
Boc-Hyp(Bzl)-OH ≥98.0% (HPLC) 15535 5g $261
Boc-O-benzyl-L-trans-4-hydroxyproline 264602 2g $360
Boc-O-benzyl-L-trans-4-hydroxyproline dicyclohexylammonium salt 99+% 236621 1g $179
BOC-HYP(BZL)-OH 95.00% AAA0000905 1G $154.35
Boc-O-benzyl-L-trans-4-hydroxyproline FB46922 5G $173
More product size

BOC-HYP(BZL)-OH Properties

Melting point ~70 °C
Boiling point 461.3±45.0 °C(Predicted)
Density 1.21±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
pka 3.75±0.40(Predicted)
form Powder
Appearance White to off-white Solid
optical activity [α]20/D 40±2°, c = 2% in ethanol
BRN 5296858
Major Application peptide synthesis
InChI 1S/C17H23NO5/c1-17(2,3)23-16(21)18-10-13(9-14(18)15(19)20)22-11-12-7-5-4-6-8-12/h4-8,13-14H,9-11H2,1-3H3,(H,19,20)/t13-,14+/m1/s1
InChIKey DGIGGVANZFKXLS-KGLIPLIRSA-N
SMILES CC(C)(C)OC(=O)N1C[C@@H](C[C@H]1C(O)=O)OCc2ccccc2
CAS DataBase Reference 54631-81-1(CAS DataBase Reference)
UNSPSC Code 12352200
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
PPE Eyeshields, Gloves, type N95 (US)
WGK Germany  3
Storage Class 13 - Non Combustible Solids

BOC-HYP(BZL)-OH price More Price(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 15535 Boc-Hyp(Bzl)-OH ≥98.0% (HPLC) 54631-81-1 5g $261 2022-05-15 Buy
Usbiological 264602 Boc-O-benzyl-L-trans-4-hydroxyproline 54631-81-1 2g $360 2021-12-16 Buy
Usbiological 236621 Boc-O-benzyl-L-trans-4-hydroxyproline dicyclohexylammonium salt 99+% 54631-81-1 1g $179 2021-12-16 Buy
American Custom Chemicals Corporation AAA0000905 BOC-HYP(BZL)-OH 95.00% 54631-81-1 1G $154.35 2021-12-16 Buy
Biosynth Carbosynth FB46922 Boc-O-benzyl-L-trans-4-hydroxyproline 54631-81-1 5G $173 2021-12-16 Buy
Product number Packaging Price Buy
15535 5g $261 Buy
264602 2g $360 Buy
236621 1g $179 Buy
AAA0000905 1G $154.35 Buy
FB46922 5G $173 Buy

BOC-HYP(BZL)-OH Chemical Properties,Uses,Production

Chemical Properties

White to off-white powder

Uses

Boc-Hyp(Bzl)-OH, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance.

reaction suitability

reaction type: Boc solid-phase peptide synthesis

Synthesis

(2S,4R)-1-BOC-4-BENZYLOXY-PYRROLIDINE-2-DICARBOXYLIC ACID METHYL ESTER

136024-60-7

4-Benzyloxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester

40350-83-2

General procedure for the synthesis of 4-(benzyloxy)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid from 1-(tert-butyl) 2-methyl (2S,4R)-4-(benzyloxy)pyrrolidine-1,2-dicarboxylic acid ester: lithium hydroxide was added to a mixture of THF and H2O (60 mL, 2:1, v/v/v/v/v) of compound 2 (3.45 g, 10.29 mmol) monohydrate (1.29 g, 30.87 mmol). The reaction mixture was stirred at room temperature for 3 hours. After the completion of the reaction was monitored by TLC, the reaction mixture was concentrated under reduced pressure, acidified to pH < 7 with 1N hydrochloric acid solution and subsequently extracted with ethyl acetate (3 x 30 mL). The organic layers were combined, washed with saturated sodium chloride solution (30 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by grinding with pentane (20 mL) to give compound 3 (3.21 g, 97% yield) in white solid form. Mass spectrum (ESI) m/z 322 [M+H]+.

References

[1] Patent: US9994614, 2018, B2. Location in patent: Page/Page column 51; 52; 53
[2] Patent: WO2012/146666, 2012, A1. Location in patent: Page/Page column 206

BOC-HYP(BZL)-OH Preparation Products And Raw materials

Global( 154)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
+86-(0)57185586718; +8613336195806 sales@capot.com China 29735 60
GenicBio Limited
+86-21-37621270 service@genicbio.com CHINA 991 58
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29838 58
Accela ChemBio Inc.
+1-858-6993322 info@accelachem.com United States 21193 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22963 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19552 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49977 58
Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
+8613580539051 joe@yuhengpharm.com CHINA 21142 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58

View Lastest Price from BOC-HYP(BZL)-OH manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
BOC-HYP(BZL)-OH pictures 2019-07-06 BOC-HYP(BZL)-OH
54631-81-1
US $100.00 / KG 1KG 99% Customized Career Henan Chemical Co

BOC-HYP(BZL)-OH Spectrum

(4R)-1-Boc-4-(phenylmethoxy)-L-proline Boc-Hyp(Bzl)-OH >=98.0% (HPLC) BOC-HYP(BZL)-OH·DCHA,98% Boc-O-benzyl-L-trans-4-hydroxyproline≥ 98% (HPLC) Boc-L-Hyp(Bzl)-OH·DCHA Boc-O-benzyl-L-trans-4-hydroxyproline dicyclohexylammonium salt99% T-BUTYLOXYCARBONYL-O-BENZYL-L-HYDROXYPROLINE 4-hydroxypyrrolidine-1,2-dicarboxylic acid O1-tert-butyl ester O2-(phenylmethyl) ester N-ALPHA-T-BUTOXYCARBONYL-O-BENZYL-L-HYDROXYPROLINE N-ALPHA-T-BUTOXYCARBONYL-O-BENZYL-TRANS-4-HYDROXY-L-PROLINE N-ALPHA-TERT-BUTYLOXYCARBONYL-L-4-O-BENZYL-HYDROXYPROLINE BOC-PRO(4-OBZL)-OH BOC-O-BENZYL-L-4-HYDROXYPROLINE BOC-O-BENZYL-L-4-TRANS-HYDROXYPROLINE BOC-O-BENZYL-L-4-TRANS-HYDROXYPROLINE DICYCLOHEXYLAMMONIUM SALT BOC-O-BENZYL-4-HYDROXY-L-PROLINE(TRANS) BOC-O-BENZYL-4-L-HYDROXYPROLINE DICYCLOHEXYLAMMONIUM SALT BOC-O-BENZYL-L-TRANS-4-HYDROXYPROLINE BOC-O-BENZYL-L-HYDROXYPROLINE BOC-L-HYP(BZL)-OH BOC-HYP(BZL) BOC-HYP(BZL)-OH BOC-HYP(BZL)-OH DCHA BOC-HYDROXYPROLINE(BZL)-OH Boc-O-benzyl-trans-4-hydroxy-L-proline Boc-O-Benzyl-L-Hydroxyproline Dicyclohexylammonium Salt N-ALPHA-T-BUTYLOXYCARBONYL-L-4-O-BENZYL-HYDROXYPROLINE NALPHA-tert-Butoxycarbonyl-O-benzyl-trans-4-hydroxy-L-proline N-alpha-t-Butyloxycarbonyl-4-O-benzyl-trans-L-hydroxyproline (2S,4R)-4-(benzyloxy)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid (Tert-Butoxy)Carbonyl Hyp(Bzl)-OH 1,2-Pyrrolidinedicarboxylic acid, 4-(phenylmethoxy)-, 1-(1,1-dimethylethyl) ester, (2S,4R)- (2S,4R)-4-(Benzyloxy)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylicaci BOC-HYP(BZL)-OH USP/EP/BP Boc-Hyp(Bzl)·DCHA (2S,4R)-N-Boc-4-(benzyloxy)pyrrolidine-2-carboxylic Acid 54631-81-1 54631-81-8 C29H46N2O5 C17H23NO5C12H23N Specialty Synthesis Proline Derivatives Peptide Synthesis Unnatural Amino Acid Derivatives Hydroxyproline [Hyp] Unusual Amino Acids Boc-Amino acid series Amino Acid Derivatives Amino Acids