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CAS

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1403684-13-8

(2S,3R)-2-(1,3-benzothiazol-2-yl)-3-(4-bromophenyl)-N,N-dimethyl-4-nitrobutanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1403684-13-8 Structure

  • Basic information

    1. Product Name: (2S,3R)-2-(1,3-benzothiazol-2-yl)-3-(4-bromophenyl)-N,N-dimethyl-4-nitrobutanamide
    2. Synonyms:
    3. CAS NO:1403684-13-8
    4. Molecular Formula:
    5. Molecular Weight: 448.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1403684-13-8.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: (2S,3R)-2-(1,3-benzothiazol-2-yl)-3-(4-bromophenyl)-N,N-dimethyl-4-nitrobutanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3R)-2-(1,3-benzothiazol-2-yl)-3-(4-bromophenyl)-N,N-dimethyl-4-nitrobutanamide(1403684-13-8)
    11. EPA Substance Registry System: (2S,3R)-2-(1,3-benzothiazol-2-yl)-3-(4-bromophenyl)-N,N-dimethyl-4-nitrobutanamide(1403684-13-8)

  • 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: 1403684-13-8(Hazardous Substances Data)

1403684-13-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403684-13-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,6,8 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1403684-13:
(9*1)+(8*4)+(7*0)+(6*3)+(5*6)+(4*8)+(3*4)+(2*1)+(1*3)=138
138 % 10 = 8
So 1403684-13-8 is a valid CAS Registry Number.

1403684-13-8Upstream product

1403684-13-8Downstream Products

1403684-13-8Relevant articles and documents

Enantioselective nickel-catalyzed Michael additions of azaarylacetates and acetamides to nitroalkenes

Fallan, Charlene,Lam, Hon Wai

, p. 11214 - 11218 (2012)

Put a nickel in it: Azaarylacetates and acetamides, which have been neglected as substrates in catalytic asymmetric synthesis, undergo highly enantioselective Michael additions to nitroalkenes in the presence of a chiral nickel(II)-bis(diamine) complex (see scheme; Bn=benzyl, MS=molecular sieves). This process is tolerant of a wide variety of azaarenes in the pronucleophile. Copyright

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