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Merck
CN

215163

氯乙酸酐

95%

别名:

一氯乙酸酐

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关于此项目

线性分子式:
(ClCH2CO)2O
化学文摘社编号:
分子量:
170.98
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-794-2
Beilstein/REAXYS Number:
774533
MDL number:
Assay:
95%
Form:
solid
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vapor pressure

<0.75 mmHg ( 20 °C)

Quality Level

assay

95%

form

solid

bp

120-123 °C/20 mmHg (lit.)

mp

48-60 °C (lit.)

solubility

chloroform: soluble 100 mg/mL, clear, colorless to faintly yellow

functional group

anhydride, chloro, ester

SMILES string

ClCC(=O)OC(=O)CCl

InChI

1S/C4H4Cl2O3/c5-1-3(7)9-4(8)2-6/h1-2H2

InChI key

PNVPNXKRAUBJGW-UHFFFAOYSA-N

Application

氯乙酸酐已用于合成:
  • 3,3′-(磺酸根)-4,4′-(氯乙酰氨基)偶氮苯(BSBCA),一种水溶性、,硫醇反应性和光控交联剂
  • D,L-7-氮杂色氨酸(D,L-7AW)
  • 2-甲基-[3,4-二-O-乙酰基-6-O-(氯乙酰基)-1,2-二脱氧-α-D-连翘苷] - [2′,1′:4,5]-2-唑啉


pictograms

Skull and crossbonesCorrosion

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

289.4 °F - closed cup

flash_point_c

143 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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K L Matta et al.
Carbohydrate research, 51(2), 215-222 (1976-11-01)
The use of the chloroacetyl group as a protecting group has been studied for a 2-methylglyco-[2',1':4,5]-2-oxazoline. The reaction of chloroacetyl chloride or chloroacetic anhydride with 2-acetamido-1,3,4-tri-O-acetyl-2-deoxy-beta-D-glucopyranose provided 2-acetamido-1,3,4-tri-O-acetyl-6-O-(chloroacetyl)-2-deoxy-beta-D-glucopyranose which, on treatment with anhydrous ferric chloride in dichloromethane, produced the desired
J D Brennan et al.
Analytical biochemistry, 252(2), 260-270 (1997-11-05)
The reaction of D,L-7-azatryptophan (D,L-7AW) with tryptophanyl-tRNA synthetase (TrpRS), adenosine triphosphate (ATP), and Mg2+ in the presence of inorganic pyrophosphatase results in the formation of a highly fluorescent l-7AW-adenylate complex. Detection of this complex is based on its enhanced fluorescence
Darcy C Burns et al.
Nature protocols, 2(2), 251-258 (2007-04-05)
This protocol describes a procedure for the synthesis of 3,3'-bis(sulfonato)-4,4'-bis(chloroacetamido)azobenzene (BSBCA), a water-soluble, thiol-reactive, photo-switchable cross-linker. In addition, a protocol is outlined for installing the cross-linker in an intramolecular fashion onto proteins bearing two surface-exposed Cys residues. BSBCA is designed



全球贸易项目编号

货号GTIN
215163-100G04061831828863
215163-25G04061838773487