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CAS

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158870-93-0

(S)-3-<(2,6-dimethylphenyl)thio>-1,2-propanediol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 158870-93-0 Structure

  • Basic information

    1. Product Name: (S)-3-<(2,6-dimethylphenyl)thio>-1,2-propanediol
    2. Synonyms:
    3. CAS NO:158870-93-0
    4. Molecular Formula:
    5. Molecular Weight: 212.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 158870-93-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-3-<(2,6-dimethylphenyl)thio>-1,2-propanediol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-<(2,6-dimethylphenyl)thio>-1,2-propanediol(158870-93-0)
    11. EPA Substance Registry System: (S)-3-<(2,6-dimethylphenyl)thio>-1,2-propanediol(158870-93-0)

  • 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: 158870-93-0(Hazardous Substances Data)

158870-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158870-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,8,7 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 158870-93:
(8*1)+(7*5)+(6*8)+(5*8)+(4*7)+(3*0)+(2*9)+(1*3)=180
180 % 10 = 0
So 158870-93-0 is a valid CAS Registry Number.

158870-93-0Downstream Products

158870-93-0Relevant articles and documents

Retention of Configuration in the Ritter-type Substitution Reaction of Chiral β-Arylthio Alcohols through the Anchimeric Assistance of the Arylthio Group

Toshimitsu, Akio,Hirosawa, Chitaru,Tamao, Kohei

, p. 8997 - 9008 (2007/10/02)

In chiral alcohols bearing a phenylthio group at the β carbon atom, the hydroxy group is replaced by nitriles through the anchimeric assistance of the phenylthio group to afford chiral amides with retention of configuration.This stereospecific Ritter-type

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