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CAS

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144846-59-3

methyl (1S,6R)-1-cyano-3,4-dimethyl-6-phenyl-3-cyclohexen-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144846-59-3 Structure

  • Basic information

    1. Product Name: methyl (1S,6R)-1-cyano-3,4-dimethyl-6-phenyl-3-cyclohexen-1-carboxylate
    2. Synonyms:
    3. CAS NO:144846-59-3
    4. Molecular Formula:
    5. Molecular Weight: 269.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144846-59-3.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: methyl (1S,6R)-1-cyano-3,4-dimethyl-6-phenyl-3-cyclohexen-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (1S,6R)-1-cyano-3,4-dimethyl-6-phenyl-3-cyclohexen-1-carboxylate(144846-59-3)
    11. EPA Substance Registry System: methyl (1S,6R)-1-cyano-3,4-dimethyl-6-phenyl-3-cyclohexen-1-carboxylate(144846-59-3)

  • 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: 144846-59-3(Hazardous Substances Data)

144846-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144846-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,4 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144846-59:
(8*1)+(7*4)+(6*4)+(5*8)+(4*4)+(3*6)+(2*5)+(1*9)=153
153 % 10 = 3
So 144846-59-3 is a valid CAS Registry Number.

144846-59-3Downstream Products

144846-59-3Relevant articles and documents

Reaction of 2,3-Dimethyl-1,3-Butadiene with Chiral (E)-2-Cyanocinnamates.

Avenoza, A.,Cativiela, C.,Mayoral, J. A.,Peregrina, J. M.

, p. 913 - 919 (2007/10/02)

The reactions of 2,3-dimethyl-1,3-butadiene with (E)-2-cyanocinnamates of (S)-ethyl lactate (1a) and (R)-pantolactone (1b), catalysed by TiCl4, afford enantiomerically pure cycloadducts which are easily converted into enantiomers (1R, 6S) and (1S, 6R) of

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