927-55-9 (4,6-二甲基苯并噻唑,4-Amino-1-pentanol)

CAS号:
927-55-9
中文名称:
4,6-二甲基苯并噻唑
英文名称:
4-Amino-1-pentanol
分子式:
C5H13NO
分子量:
103.162821531296

4,6-二甲基苯并噻唑(927-55-9)名称与标识符

名称

中文别名:
4-氨基-1-戊醇;4,6-二甲基苯并噻唑;
英文别名:
1-Pentanol, 4-amino-;4-Amino-1-pentanol;4-AMINO-1-PENTANOL,PALE YELLOW LOW MELTING SOLID;4-aminopentan-1-ol;1-Pentanol,4-amino;4-Amino-pentan-1-ol;4-Amino-pentanol;4-Hydroxy-1-methyl-butylamin;4-hydroxy-1-methyl-butylamine;4-Amino-1-pentanol (ACI);NSC 1095;(4S)-4-aminopentan-1-ol;DTXSID401316181;1-Pentanol,4-amino-;NS00042621;927-55-9;NSC1095;SB84011;1630497-31-2;(4R)-4-aminopentan-1-ol;SCHEMBL362003;AKOS006339189;MFCD16251198;Z1203578676;AT20758;DB-295100;EINECS 213-151-4;NSC-1095;EN300-104358;

标识符

InChIKey:
JAXJUENAJXWFBX-UHFFFAOYSA-N
Inchi:
1S/C5H13NO/c1-5(6)3-2-4-7/h5,7H,2-4,6H2,1H3
SMILES:
OCCCC(C)N

4,6-二甲基苯并噻唑(927-55-9)物化性质

实验特性

  • LogP : 0.80640
  • PSA : 46.25000
  • 折射率 : 1.449
  • 沸点 : 117-119°C/25 mm
  • 熔点 : 32°C
  • 闪点 : 59.4°C
  • 密度 : 0.915

计算特性

  • 精确分子量 : 103.10000
  • 氢键供体数量 : 2
  • 氢键受体数量 : 2
  • 可旋转化学键数量 : 3
  • 同位素质量 : 103.1
  • 重原子数量 : 7
  • 复杂度 : 39.1
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 1
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : -0.3
  • 拓扑分子极性表面积 : 46.2A^2

4,6-二甲基苯并噻唑(927-55-9)海关数据

海关编码:
2922199090
海关数据:

中国海关编码:

2922199090

概述:

2922199090. 其他氨基醇及其醚,酯和它们的盐(但含一种以上含氧基的除外). 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:30.0%

申报要素:

品名, 成分含量, 用途, 乙醇胺及其盐应报明色度, 乙醇胺及其盐应报明包装

Summary:

2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

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4,6-二甲基苯并噻唑(927-55-9)合成路线

合成路线:1 步
反应条件:
参考文献:
Reductive amination of bio-based 2-hydroxytetrahydropyran to 5-Amino-1-pentanol over nano-Ni-Al2O3 catalysts
Zhang, Jia; Yang, Jian; Tian, Junying; Liu, Hailong; Li, Xuemei; et al, New Journal of Chemistry, 2021, 45(9), 4236-4245
合成路线:1 步
反应条件:
参考文献:
Synthesis of deuterium labelled chloroquine, hydroxychloroquine and their metabolites
Tian, Lei; Zhang, Chi; Li, Jian, Journal of Chemical and Pharmaceutical Research, 2013, 5(10), 396-401
合成路线:1 步
反应条件:
参考文献:
Efficient Synthesis of Pharmaceutical Intermediates from Biomass-Derived Aldehydes and Ketones over Robust NixAl Nanocatalysts
Zhang, Jia; Yang, Jian; Li, Xuemei; Liu, Hailong; Wang, Aiqin ; et al, ACS Sustainable Chemistry & Engineering, 2022, 10(17), 5526-5537
合成路线:1 步
反应条件:
参考文献:
Preparation of quinazoline derivatives as cytokines TNF-α, IL-6 and IL-1β inhibitors for prevention and/or treatment of TNF-α, IL-6 and IL-1β-related diseases
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Functionalization of the δ-carbon atom by the ferrous ion induced decomposition of alkyl hydroperoxides in the presence of cupric salts
Cekovic, Zivorad; Cvetkovic, Milutin, Tetrahedron Letters, 1982, 23(37), 3791-4
合成路线:1 步
反应条件:
参考文献:
Further syntheses of primaquine analogs
Elderfield, Robert C.; Claflin, Elizabeth F.; Mertel, Holly E.; McCurdy, Orville L.; Mitch, Richard T.; et al, Journal of the American Chemical Society, 1955, 77, 4819-22
合成路线:1 步
反应条件:
参考文献:
Preparation of heteroaryl compounds as autophagy and histone deactylases inhibitors
, World Intellectual Property Organization, , ,
合成路线:1 步
参考文献:
Heterocyclic compounds and their use as pesticides
, South Africa, , ,
合成路线:1 步
参考文献:
8-Quinolinamine derivatives
, United States, , ,
合成路线:1 步
参考文献:
Piperidine alkaloids. IV. New synthesis of (±)-solenopsine A by heterocyclization-aminomercuration
Moriyama, Yoshiko; Doan Huyhn Dong; Monneret, Claud; Khuong Huu Qui, Tetrahedron Letters, 1977, (10), 825-8
合成路线:1 步
参考文献:
Synthesis of N1-(6-methoxy-8-quinolinyl)-1,4-pentanediamine dihydrochloride (quinocide)
Mikhlina, E. E.; Yanina, A. D.; Vorob'eva, V. Ya.; Tsizin, Yu. S.; Komarova, N. A.; et al, Khimiko-Farmatsevticheskii Zhurnal, 1973, 7(10), 3-6
合成路线:1 步
反应条件:
参考文献:
Rh-Catalyzed Hydrogenation of Amino Acids to Biobased Amino Alcohols: Tackling Challenging Substrates and Application to Protein Hydrolysates
Vandekerkhove, Annelies ; Claes, Laurens ; De Schouwer, Free; Van Goethem, Cedric ; Vankelecom, Ivo F. J.; et al, ACS Sustainable Chemistry & Engineering, 2018, 6(7), 9218-9228
合成路线:1 步
反应条件:
参考文献:
Production of functionalized carboxylic acids and alcohols by reverse fatty acid oxidation in metabolically engineered microorganisms
, United States, , ,

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