5856-82-6 (丁酰溴,Butanoyl bromide)

快速询单

结构式：

丁酰溴MOL文件

CAS号：

5856-82-6

中文名称：

丁酰溴

英文名称：

Butanoyl bromide

分子式：

C₄H₇BrO

分子量：

151.001780748367

API：

Procaterol

丁酰溴(5856-82-6)名称与标识符

名称

中文别名：

丁基溴;丁酰溴;

英文别名：

Butanoyl bromide;BUTYRYL BROMIDE;2-bromobutyraldehyde;Buttersaeurebromid;butyric acid bromide;Butyrylbromid;I14-9612;n-butyryl bromide;5856-82-6;DTXSID10468738;FT-0623351;SCHEMBL873391;AKOS015917500;BUTYRYLBROMIDE;

标识符

InChIKey：

QAWBXZYPFCFQLA-UHFFFAOYSA-N

Inchi：

1S/C4H7BrO/c1-2-3-4(5)6/h2-3H2,1H3

SMILES：

BrC(CCC)=O

丁酰溴(5856-82-6)物化性质

实验特性

LogP : 1.70800
PSA : 17.07000
折射率 : 1.5960
沸点 : 129°C (rough estimate)
密度 : 1.4162

计算特性

精确分子量 : 149.96800
氢键供体数量 : 0
氢键受体数量 : 1
可旋转化学键数量 : 2
同位素质量 : 149.96803g/mol
重原子数量 : 6
复杂度 : 51.5
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 : 0
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） : 1.7
拓扑分子极性表面积 : 17.1Å²

丁酰溴(5856-82-6)推荐厂家更多厂家(1)

公司名称	手机号/电话	联系人	QQ	微信	询单
金锦乐（湖南）化学有限公司		金锦乐	1226360695		询单

丁酰溴(5856-82-6)相关文献

1. ATRP-mediated continuous assembly of polymers for the preparation of nanoscale films
Damien Mertz,Christopher J. Ochs,Zhiyuan Zhu,Lillian Lee,Stefanie N. Guntari,Georgina K. Such,Tor Kit Goh,Luke A. Connal,Anton Blencowe,Greg G. Qiao,Frank Caruso Chem. Commun. 2011 47 12601
2. Biomimetic star-shaped poly(ε-caprolactone)-b-glycopolymer block copolymers with porphyrin-core for targeted photodynamic therapy
Xiao-Hui Dai,Zhi-Ming Wang,Ya-fei Huang,Jian-Ming Pan,Yong-sheng Yan,Dong-Ming Liu,Lin Sun RSC Adv. 2014 4 42486
3. Some recent developments of polyhedral oligomeric silsesquioxane (POSS)-based polymeric materials
FuKe Wang,Xuehong Lu,Chaobin He J. Mater. Chem. 2011 21 2775
4. Soft polymeric nanoparticle additives for next generation gas separation membranes
Andri Halim,Qiang Fu,Qiwyn Yong,Paul A. Gurr,Sandra E. Kentish,Greg G. Qiao J. Mater. Chem. A 2014 2 4999
5. 530. Quinolizines. Part. VII. Rearrangement products from 1,2,3,4-tetrahydro-1-hydroxyiminoquinolizinium bromides
A. Fozard,Gurnos Jones J. Chem. Soc. 1964 2763
6. Acylation. Part XXVIII. The kinetics and mechanism of the addition of hydrogen halides to dimethylketen in ether solution. Relative reactivities of substrates towards ketens and a comparison with mechanism of acylation by other acylating agents in non-hydroxylic solvents
P. J. Lillford,D. P. N. Satchell J. Chem. Soc. B 1968 897
7. 719. Acylation. Part XIII. Kinetics and mechanism of the reaction of phenols with acyl bromides in acetonitrile
J. M. Briody,D. P. N. Satchell J. Chem. Soc. 1964 3724
8. Halogen mobility in S N2 reactions of carbonyl compounds. Comparisons with aromatic halogen mobility
Joseph Miller,Oi-Ling Ying N2 reactions of carbonyl compounds. Comparisons with aromatic halogen mobility. Joseph Miller Oi-Ling Ying J. Chem. Soc. Perkin Trans. 2 1985 323
9. Organic chemistry
J. Chem. Soc. Abstr. 1924 126 i1157
10. Organic chemistry
J. Chem. Soc. Abstr. 1912 102 i149

116464-23-4(11-bromoundecanoyl bromide) 80379-10-8((S)-1-(2-硝基苯基)乙醇) 8039-11-0(2-octyldodecan-1-ol) 80563-82-2(二甲氧基苯磺酰氯) 80563-87-7(Methyl 2-chloro-6-nitrobenzoate) 80538-72-3(4-乙酰-烟酰胺) 80543-51-7(O-FORMYLMANDELOYL CHLORIDE) 80584-92-5(三嗪聚羧酸三乙醇胺盐 Irgacor L184)