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S-benzyl carbonochloridothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 37734-45-5 Structure
  • Basic information

    1. Product Name: S-benzyl carbonochloridothioate
    2. Synonyms: 37734-45-5; S-benzyl chlorothiocarbonate
    3. CAS NO:37734-45-5
    4. Molecular Formula: C8H7ClOS
    5. Molecular Weight: 186.6586
    6. EINECS: 609-472-8
    7. Product Categories: N/A
    8. Mol File: 37734-45-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 260.3°C at 760 mmHg
    3. Flash Point: 111.2°C
    4. Appearance: N/A
    5. Density: 1.289g/cm3
    6. Vapor Pressure: 0.0123mmHg at 25°C
    7. Refractive Index: 1.587
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: S-benzyl carbonochloridothioate(CAS DataBase Reference)
    11. NIST Chemistry Reference: S-benzyl carbonochloridothioate(37734-45-5)
    12. EPA Substance Registry System: S-benzyl carbonochloridothioate(37734-45-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 37734-45-5(Hazardous Substances Data)

37734-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37734-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,3 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37734-45:
(7*3)+(6*7)+(5*7)+(4*3)+(3*4)+(2*4)+(1*5)=135
135 % 10 = 5
So 37734-45-5 is a valid CAS Registry Number.

37734-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name S-benzyl chloromethanethioate

1.2 Other means of identification

Product number -
Other names thiocarbonochloridic acid S-benzyl ester

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:37734-45-5 SDS

37734-45-5Relevant articles and documents

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.

Antipicornaviral compounds compositions containing them and methods for their use

-

, (2008/06/13)

Picornaviral 3C protease inhibitors, obtainable by chemical synthesis, inhibit or block the biological activity of the picornaviral 3C protease. These compounds, as well as pharmaceutical compositions that contain these compounds, are suitable for treatin

Antipicornaviral compounds and methods for their use and preparation

-

, (2008/06/13)

Picornaviral 3C protease inhibitors, obtainable by chemical synthesis, inhibit or block the biological activity of picornaviral 3C proteases. These compounds, as well as pharmaceutical compositions that contain these compounds, are suitable for treating patients or hosts infected with one or more picornaviruses. Several novel methods and intermediates can be used to prepare the novel picornaviral 3C protease inhibitors of the present invention.

Method for preparation of benzyl mercaptan

-

, (2008/06/13)

A method for the preparation of benzyl mercaptan is disclosed which comprises reacting a benzyl halide of the formula STR1 wherein X is chlorine or bromine, with an alkali metal hydrosulfide salt, at a temperature and for a sufficient period of time to ca

1-(N-Octylthiocarbonyl)-2-(4-thiazolyl)benzimidazole

-

, (2008/06/13)

New benzimidazoles substituted at the 1-position with carbonyl substituents and at the 2-position with a 4-thiazolyl group are effective fungicides and anthelmintics. The compounds as well as processes for their preparation are described along with antifungal and anthelmintic compositions for their use. The 1-position substituent is a hydrocarbon group of from 5 to 12 carbon atoms connected to the carbonyl group through an oxygen or a sulfur atom. The compounds are generally prepared by contacting a 1-unsubstituted benzimidazole with a hydrocarbon radical substituted chloroformate or chlorothiol formate.

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