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S-TERT-BUTYL CHLOROTHIOFORMATE, 96% is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13889-95-7

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13889-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13889-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,8 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13889-95:
(7*1)+(6*3)+(5*8)+(4*8)+(3*9)+(2*9)+(1*5)=147
147 % 10 = 7
So 13889-95-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H9ClOS/c1-5(2,3)8-4(6)7/h1-3H3

13889-95-7 Well-known Company Product Price

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  • Aldrich

  • (672939)  S-tert-Butylchlorothioformate  96%

  • 13889-95-7

  • 672939-5G

  • 1,421.55CNY

  • Detail

13889-95-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name S-tert-butyl chloromethanethioate

1.2 Other means of identification

Product number -
Other names S-tert-Butyl chlorothioformate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13889-95-7 SDS

13889-95-7Relevant academic research and scientific papers

S-alkyl chlorothioformates from xanthates

Gade, Alexandra M.,Abelt, Christopher J.

, p. 2097 - 2099 (2008/02/12)

Reaction of S-alkyl O-ethyl xanthates (S-alkyl O-ethyl dithiocarbonates) with catalytic Vilsmeier reagent generated in situ from N-formylmorpholine (morpholine-4-carbaldehyde) gives S-alkyl chlorothioformates in good yields. Georg Thieme Verlag Stuttgart.

New heterocyclic precursors for thermal generation of reactive, electron-rich 1,2-diaza-1,3-butadienes

Boeckman Jr., Robert K.,Ge, Ping,Reed, Jessica E.

, p. 3647 - 3650 (2007/10/03)

Figure presented The preparation and thermolysis of new stable heterocyclic precursors of 1,2-diaza-1,3-butadienes is described. The resulting reactive diazadienes are trapped in situ with N-phenyldiazamaleimide. The effect of precursor structure on the temperature at which the diazadienes are generated is discussed.

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