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135895

Sigma-Aldrich

Dimethylthiocarbamoyl chloride

97%

동의어(들):

1-Chloro-N,N-dimethylthioformamide

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모든 사진(3)

About This Item

Linear Formula:
(CH3)2NCSCl
CAS Number:
16420-13-6
Molecular Weight:
123.60
Beilstein:
635823
EC Number:
240-468-5
MDL number:
MFCD00004919
UNSPSC 코드:
12352100
PubChem Substance ID:
24848243
NACRES:
NA.22

Quality Level

100

분석

97%

형태

solid

bp

90-95 °C/0.5 mmHg (lit.)

mp

39-43 °C (lit.)

solubility

chloroform: soluble 100 mg/mL, clear to very slightly hazy, very faintly yellow

작용기

amine
chloro

저장 온도

2-8°C

SMILES string

CN(C)C(Cl)=S

InChI

1S/C3H6ClNS/c1-5(2)3(4)6/h1-2H3

InChI key

PHWISQNXPLXQRU-UHFFFAOYSA-N

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애플리케이션

Dimethylthiocarbamoyl chloride was used in chemoselective deoxygenation of pyridine-N-oxides. It was used in the synthesis of (±)-thia-calanolide A. It was used as starting reagent in the synthesis of dimethylthiocarbamates.

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point (°F)

208.4 °F - closed cup

Flash Point (°C)

98 °C - closed cup

개인 보호 장비

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

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
MKCQ1218
MKCM5395
MKCJ9700
MKCJ0793
MKCG9318

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

COA 검색

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Journal of Heterocyclic Chemistry, 44, 487-487 (2007)
D K Barma et al.
Organic letters, 5(25), 4755-4757 (2003-12-05)
Dimethylthiocarbamates (DMTCs), prepared from the corresponding alcohols using commercial dimethylthiocarbamoyl chloride, are spectrally simple, achiral, and nonpolar. DMTCs are moderately to highly stable to a wide range of reagents and conditions including metal hydrides, hydroboration, ylides, NaOH, HCl, organolithiums, Grignards
A synthesis of (?)-thia-calanolide A, its resolution and in vitro biological evaluation.
Chopade AU, et al. et al.
Arabian Journal of Chemistry (2012)
Harley D Betts et al.
Molecules (Basel, Switzerland), 25(19) (2020-10-07)
Silver(I)-based coordination polymers or metal-organic frameworks (MOFs) display useful antibacterial properties, whereby distinct materials with different bonding can afford control over the release of silver(I) ions. Such silver(I) materials are comprised of discrete secondary building units (SBUs), and typically formed

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