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178681-82-8

(1R,9S)-10-Acetyl-4-methoxy-1-methyl-10-aza-tricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-8-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 178681-82-8 Structure

  • Basic information

    1. Product Name: (1R,9S)-10-Acetyl-4-methoxy-1-methyl-10-aza-tricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-8-one
    2. Synonyms:
    3. CAS NO:178681-82-8
    4. Molecular Formula:
    5. Molecular Weight: 259.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 178681-82-8.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,9S)-10-Acetyl-4-methoxy-1-methyl-10-aza-tricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-8-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,9S)-10-Acetyl-4-methoxy-1-methyl-10-aza-tricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-8-one(178681-82-8)
    11. EPA Substance Registry System: (1R,9S)-10-Acetyl-4-methoxy-1-methyl-10-aza-tricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-8-one(178681-82-8)

  • 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: 178681-82-8(Hazardous Substances Data)

178681-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178681-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,6,8 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 178681-82:
(8*1)+(7*7)+(6*8)+(5*6)+(4*8)+(3*1)+(2*8)+(1*2)=188
188 % 10 = 8
So 178681-82-8 is a valid CAS Registry Number.

178681-82-8Relevant articles and documents

Asymmetric synthesis of benzylic quaternary carbon center via an enzymatic reaction

Shiotani, Shunsaku,Okada, Hirohiko,Nakamata, Kumiko,Yamamoto, Takako,Sekino, Fumie

, p. 1031 - 1047 (2007/10/03)

(R)-(+)- ((R)-(+)-12) and(S)-(-)-1-formyl-1-methyl-7-methoxy-1,2,3,4-tetrahydronaphthalene((S)-(-)-12) were synthesized based on enantioselective PLE hydrolysis of diethyl 2-(m-methoxyphenyl)-2-methylmalonate. From (R)-(+)-12, (+)-O-Methylaphanorphine (16

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