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Merck
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주요 문서

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310670

Sigma-Aldrich

Oxalyl chloride solution

2.0 M in methylene chloride

동의어(들):

Dichlorooxalic acid, Ethanedioyl chloride, Oxalic acid chloride, Oxalic acid dichloride, Oxalic dichloride, Oxaloyl chloride, Oxaloyl dichloride, Oxalyl dichloride

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About This Item

Linear Formula:
ClCOCOCl
CAS Number:
79-37-8
Molecular Weight:
126.93
Beilstein:
1361988
MDL number:
MFCD00000704
UNSPSC 코드:
12352106
PubChem Substance ID:
24858810
NACRES:
NA.22

양식

liquid

반응 적합성

reagent type: oxidant

농도

2.0 M in methylene chloride

density

1.335 g/mL at 25 °C

작용기

acyl chloride

SMILES string

ClC(=O)C(Cl)=O

InChI

1S/C2Cl2O2/c3-1(5)2(4)6

InChI key

CTSLXHKWHWQRSH-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

Oxalyl chloride is generally used as a dimethyl sulfoxide activator and a chlorinating agent to convert carboxylic acid to acid chlorides.

신호어

Danger

유해 및 위험 성명서

H260,H302,H314,H331,H336,H351

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3 - Water-react 1

표적 기관

Central nervous system

보충제 위험성

EUH014,EUH029,EUH071

Storage Class Code

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

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

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
MKCP6787
SHBK6285
BCBJ7788V
SHBJ4925
SHBF0926V

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Synthesis and characterization of highly soluble and heat stable new poly (amide-ether) s containing pyridine rings in the main chain.
Banihashemi A and Vakili MR
e-Polymers, 8(1) (2008)
Catalytic syntheses of N-heterocyclic ynones and ynediones by in situ activation of carboxylic acids with oxalyl chloride.
Christina Boersch et al.
Angewandte Chemie (International ed. in English), 50(44), 10448-10452 (2011-09-13)
Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide" activated" by oxalyl chloride.
Mancuso AJ, et al.
The Journal of Organic Chemistry, 43(12), 2480-2482 (1978)
Benoît Heurtaux et al.
The Journal of organic chemistry, 70(4), 1474-1477 (2005-02-12)
[reaction: see text] Several natural pulvinic acids were synthesized. Silyl ketene acetals derived from methyl arylacetates (4 equiv) reacted with oxalyl chloride at -78 degrees C, without the need of adding a catalyst. After treatment of the crude diketones with
Peter J Manley et al.
Organic letters, 4(18), 3127-3129 (2002-08-31)
[reaction: see text] A mild, practical, one-pot method for the generation of imidoyl chlorides and their subsequent in situ reaction with pyridine-1-oxides is described. The imidoyl chlorides were formed from the reaction of secondary amides with a stoichiometric amount of
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