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CAS

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1402449-16-4

(R)-3-((2-aminophenyl)thio)-3-(4-methoxyphenyl)-N,N-dimethylpropanethioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1402449-16-4 Structure

  • Basic information

    1. Product Name: (R)-3-((2-aminophenyl)thio)-3-(4-methoxyphenyl)-N,N-dimethylpropanethioamide
    2. Synonyms: (R)-3-((2-aminophenyl)thio)-3-(4-methoxyphenyl)-N,N-dimethylpropanethioamide
    3. CAS NO:1402449-16-4
    4. Molecular Formula:
    5. Molecular Weight: 346.517
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1402449-16-4.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: (R)-3-((2-aminophenyl)thio)-3-(4-methoxyphenyl)-N,N-dimethylpropanethioamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-3-((2-aminophenyl)thio)-3-(4-methoxyphenyl)-N,N-dimethylpropanethioamide(1402449-16-4)
    11. EPA Substance Registry System: (R)-3-((2-aminophenyl)thio)-3-(4-methoxyphenyl)-N,N-dimethylpropanethioamide(1402449-16-4)

  • 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: 1402449-16-4(Hazardous Substances Data)

1402449-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402449-16-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,4,4 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1402449-16:
(9*1)+(8*4)+(7*0)+(6*2)+(5*4)+(4*4)+(3*9)+(2*1)+(1*6)=124
124 % 10 = 4
So 1402449-16-4 is a valid CAS Registry Number.

1402449-16-4Upstream product

1402449-16-4Downstream Products

1402449-16-4Relevant articles and documents

Catalytic asymmetric conjugate addition of thiols to α,β- unsaturated thioamides: Expeditious access to enantioenriched 1,5-benzothiazepines

Ogawa, Takanori,Kumagai, Naoya,Shibasaki, Masakatsu

, p. 8551 - 8554 (2012)

Softly does it: The title reaction proceeded under proton transfer conditions with a catalyst prepared from commercially available reagents to afford the desired product in high enantioselectivity. The reaction was compatible with a free amino group, thus allowing for expeditious access to enantiomerically enriched 1,5-benzothiazepines, which are important chemical entities in medicinal chemistry.

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