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104197-96-8

(1R,2S,5R)-2-tert-butyl-5-methylcyclohexyl bromoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104197-96-8 Structure

  • Basic information

    1. Product Name: (1R,2S,5R)-2-tert-butyl-5-methylcyclohexyl bromoacetate
    2. Synonyms:
    3. CAS NO:104197-96-8
    4. Molecular Formula:
    5. Molecular Weight: 291.228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104197-96-8.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: (1R,2S,5R)-2-tert-butyl-5-methylcyclohexyl bromoacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2S,5R)-2-tert-butyl-5-methylcyclohexyl bromoacetate(104197-96-8)
    11. EPA Substance Registry System: (1R,2S,5R)-2-tert-butyl-5-methylcyclohexyl bromoacetate(104197-96-8)

  • 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: 104197-96-8(Hazardous Substances Data)

104197-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104197-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,9 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104197-96:
(8*1)+(7*0)+(6*4)+(5*1)+(4*9)+(3*7)+(2*9)+(1*6)=118
118 % 10 = 8
So 104197-96-8 is a valid CAS Registry Number.

104197-96-8Relevant articles and documents

Auxiliary Structure and Asymmetric Induction in the Ene Reactions of Chiral Glyoxylates

Whitesell, James K.,Lawrence, Robert M.,Chen, Huang-Hsing

, p. 4779 - 4784 (2007/10/02)

A variety of chiral auxiliares (1a-13a) were prepared and tested for levels of asymmetric induction control in the ene reaction of chiral glyoxylates.Structural features required for high levels of control were defined by systematic modification of the auxiliary, providing systems with induction levels that ranged from 1.2 to 1 to better than 99.9 to 0.1.

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