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1268464-31-8

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  • 1268464-31-8 Structure

  • Basic information

    1. Product Name: (3R)-3-nitromethyl-1-phenyl-2-(phenylsulfonyl)hexan-1-one
    2. Synonyms:
    3. CAS NO:1268464-31-8
    4. Molecular Formula:
    5. Molecular Weight: 375.445
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268464-31-8.mol
    9. Article Data: 1

  • 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: (3R)-3-nitromethyl-1-phenyl-2-(phenylsulfonyl)hexan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R)-3-nitromethyl-1-phenyl-2-(phenylsulfonyl)hexan-1-one(1268464-31-8)
    11. EPA Substance Registry System: (3R)-3-nitromethyl-1-phenyl-2-(phenylsulfonyl)hexan-1-one(1268464-31-8)

  • 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: 1268464-31-8(Hazardous Substances Data)

1268464-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268464-31-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,4,6 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1268464-31:
(9*1)+(8*2)+(7*6)+(6*8)+(5*4)+(4*6)+(3*4)+(2*3)+(1*1)=178
178 % 10 = 8
So 1268464-31-8 is a valid CAS Registry Number.

1268464-31-8Downstream Products

1268464-31-8Relevant articles and documents

Synthesis of chiral cyclic nitrones by asymmetric addition of β-ketosulfones to nitroalkenes followed by reductive cyclization

Mancheno, Olga Garci,Tangen, Pia,Rohlmann, Renate,Froehlich, Roland,Aleman, Jose

experimental part, p. 984 - 992 (2011/03/20)

The first organocatalytic addition of β-ketosulfones to nitroalkenes catalyzed by thiourea cinchona alkaloids is presented. The readily obtained addition products were selectively transformed into chiral nitrones by reduction of the nitro group and in sit

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