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S-phenyl pyrrolidine-1-carbothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138906-08-8 Structure
  • Basic information

    1. Product Name: S-phenyl pyrrolidine-1-carbothioate
    2. Synonyms:
    3. CAS NO:138906-08-8
    4. Molecular Formula: C11H13NOS
    5. Molecular Weight: 207.292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138906-08-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 327.1°C at 760 mmHg
    3. Flash Point: 151.6°C
    4. Appearance: N/A
    5. Density: 1.21g/cm3
    6. Vapor Pressure: 0.000206mmHg at 25°C
    7. Refractive Index: 1.616
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: S-phenyl pyrrolidine-1-carbothioate(CAS DataBase Reference)
    11. NIST Chemistry Reference: S-phenyl pyrrolidine-1-carbothioate(138906-08-8)
    12. EPA Substance Registry System: S-phenyl pyrrolidine-1-carbothioate(138906-08-8)
  • 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: 138906-08-8(Hazardous Substances Data)

138906-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138906-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 138906-08:
(8*1)+(7*3)+(6*8)+(5*9)+(4*0)+(3*6)+(2*0)+(1*8)=148
148 % 10 = 8
So 138906-08-8 is a valid CAS Registry Number.

138906-08-8SDS

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-phenyl pyrrolidine-1-carbothioate

1.2 Other means of identification

Product number -
Other names -

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:138906-08-8 SDS

138906-08-8Downstream Products

138906-08-8Relevant articles and documents

Achieving functional group diversity in parallel synthesis: solution-phase synthesis of a library of ureas, carbamates, thiocarbamates, and amides using carbamoylimidazolium salts

Grzyb, Justyna A.,Batey, Robert A.

, p. 5279 - 5282 (2008/12/21)

A convenient protocol for the parallel solution-phase synthesis of a library of thiocarbamates, ureas, carbamates, and amides from carbamoylimidazolium salts has been developed. The crystalline carbamoylimidazolium salts are readily synthesized from secon

A facile method for the synthesis of thiocarbamates: Palladium-catalyzed reaction of disulfide, amine, and carbon monoxide

Nishiyama, Yutaka,Kawamatsu, Hiroaki,Sonoda, Noboru

, p. 2551 - 2554 (2007/10/03)

(Equation Presented) A new method for the synthesis of thiocarbamates has been developed. When dialkyl or diaryl disulfides were allowed to react with secondary amines and carbon monoxide in the presence of a catalytic amount of a palladium complex, the thiocarbamates were obtained in moderate to good yields. In contrast to that of secondary amines, in the reaction of a primary amine, no formation of thiocarbamate was confirmed, but urea was formed in good yield.

REACTIONS OF UNSTABLE DIALKYLCARBAMOYL LITHIUMS WITH SULFUR COMPOUNDS

Mizuno, Takumi,Nishiguchi, Ikuzo,Hirashima, Tsuneaki

, p. 2403 - 2412 (2007/10/02)

Unstable dialkylcarbamoyl lithiums, generated from the reaction of lithium dialkylamides with carbon monoxide, were successfully trapped by sulfur compounds (elemental sulfur, disulfides, carbon disulfide, and carbonyl sulfide) at low temperature, through their potent affinity with a sulfur atom.These efficient reactions were also applied to development of a facile synthetic method for thiocarbamates, useful herbicides, and thiooxamates.

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