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Merck
CN

23181

氯甲酸氯甲酯

≥98.0% (GC)

别名:

1-氯甲基氯甲酸酯, 氯甲基氯化碳, 氯甲氧羰基氯, 氯甲酸氯甲酯, 氯碳酸氯甲基酯

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关于此项目

线性分子式:
ClCOOCH2Cl
化学文摘社编号:
分子量:
128.94
MDL number:
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
244-793-3
Beilstein/REAXYS Number:
506426
Assay:
≥98.0% (GC)
Form:
liquid
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Quality Level

assay

≥98.0% (GC)

form

liquid

refractive index

n20/D 1.428

bp

107-108 °C (lit.)

density

1.450 g/mL at 20 °C

functional group

chloro

storage temp.

2-8°C

SMILES string

ClCOC(Cl)=O

InChI

1S/C2H2Cl2O2/c3-1-6-2(4)5/h1H2

InChI key

JYWJULGYGOLCGW-UHFFFAOYSA-N

Application

氯甲酸氯甲基酯作为关键反应物用于合成:
  • 双氯芬酸和氟芬那酸的新型氨基羰基氧甲酯
  • 环孢菌素 A 的高水溶性单甲氧基聚乙二醇前体药物
  • 3-乙酰氧基甲氧羰基-1-芳基-3-甲基三氮烯系列


pictograms

Skull and crossbonesCorrosion

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Inhalation - 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

203.0 °F - closed cup

flash_point_c

95 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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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E Carvalho et al.
Bioorganic & medicinal chemistry, 8(7), 1719-1725 (2000-09-08)
A series of 3-acyloxymethyloxycarbonyl-1-aryl-3-methyltriazenes 5 was synthesised by the sequential reaction of 1-aryl-3-methyltriazenes with (i) chloromethyl chloroformate, (ii) NaI in dry acetone, and (iii) either the silver carboxylate or the carboxylic acids in the presence of silver carbonate. The hydrolysis
Lina Ribeiro et al.
Archiv der Pharmazie, 340(1), 32-40 (2007-01-09)
Aminocarbonyloxymethyl ester prodrugs are known to undergo rearrangement in aqueous solutions to form the corresponding N-acylamine side product via an O-->N intramolecular acyl transfer from the carbamate conjugate base. Novel aminocarbonyloxymethyl esters of diclofenac and flufenamic acid containing amino acid
Hoon Cho et al.
Archives of pharmacal research, 27(6), 662-669 (2004-07-31)
The highly water-soluble monomethoxypoly(ethyleneglycol) (mPEG) prodrugs of cyclosporin A (CsA) were synthesized. These prodrugs were prepared by initially preparing intermediate in the form of carbonate at the 3'-positions of CsA with chloromethyl chloroformate, in the presence of a base to



全球贸易项目编号

货号GTIN
23181-50ML04061836691554
23181-10ML04061836691547