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(1R,2R)-(-)-trans-4,6-dimethylcyclohex-4-ene-1,2-dicarboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1010390-97-2 Structure
  • Basic information

    1. Product Name: (1R,2R)-(-)-trans-4,6-dimethylcyclohex-4-ene-1,2-dicarboxylic acid
    2. Synonyms: (1R,2R)-(-)-trans-4,6-dimethylcyclohex-4-ene-1,2-dicarboxylic acid
    3. CAS NO:1010390-97-2
    4. Molecular Formula:
    5. Molecular Weight: 198.219
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1010390-97-2.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,2R)-(-)-trans-4,6-dimethylcyclohex-4-ene-1,2-dicarboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2R)-(-)-trans-4,6-dimethylcyclohex-4-ene-1,2-dicarboxylic acid(1010390-97-2)
    11. EPA Substance Registry System: (1R,2R)-(-)-trans-4,6-dimethylcyclohex-4-ene-1,2-dicarboxylic acid(1010390-97-2)
  • 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: 1010390-97-2(Hazardous Substances Data)

1010390-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1010390-97-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,3,9 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1010390-97:
(9*1)+(8*0)+(7*1)+(6*0)+(5*3)+(4*9)+(3*0)+(2*9)+(1*7)=92
92 % 10 = 2
So 1010390-97-2 is a valid CAS Registry Number.

1010390-97-2Downstream Products

1010390-97-2Relevant articles and documents

Asymmetric Diels-Alder reaction of 1,3-butadienes with (-)-dimenthyl fumarate in the presence of BBr3 and BBr3·OEt 2

Mamedov

, p. 184 - 187 (2007/10/03)

Asymmetric synthesis of substituted cyclohexenes was performed by [4+2]-cycloaddition of (-)-dimenthyl fumarate to 1,3-butadienes in the presence of BBr3 and BBr3·OEt2. The latter are efficient catalysts for this reaction.

Alicyclic diamine fungicides

-

, (2008/06/13)

Use of a compound having the general formula: STR1 wherein R1, R2, R3 and R4 which may be the same or different represent hydrogen atoms or alkyl groups of 1-6 carbon atoms, or NR1 R2 and/o

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