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176706-41-5

5(N-methylbenzoylamino)-2,2,6,6-tetramethylheptan-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 176706-41-5 Structure

  • Basic information

    1. Product Name: 5(N-methylbenzoylamino)-2,2,6,6-tetramethylheptan-3-ol
    2. Synonyms:
    3. CAS NO:176706-41-5
    4. Molecular Formula:
    5. Molecular Weight: 305.461
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 176706-41-5.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: 5(N-methylbenzoylamino)-2,2,6,6-tetramethylheptan-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5(N-methylbenzoylamino)-2,2,6,6-tetramethylheptan-3-ol(176706-41-5)
    11. EPA Substance Registry System: 5(N-methylbenzoylamino)-2,2,6,6-tetramethylheptan-3-ol(176706-41-5)

  • 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: 176706-41-5(Hazardous Substances Data)

176706-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176706-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,7,0 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 176706-41:
(8*1)+(7*7)+(6*6)+(5*7)+(4*0)+(3*6)+(2*4)+(1*1)=155
155 % 10 = 5
So 176706-41-5 is a valid CAS Registry Number.

176706-41-5Upstream product

176706-41-5Downstream Products

176706-41-5Relevant articles and documents

5(N-methylbenzoylamino)-2,2,6,6-tetramethylheptan-3-ol as a new class of recoverable chiral auxiliary

Yamamoto, Yoshinori,Kin, Hirofumi,Suzuki, Ichiro,Asao, Naoki

, p. 1863 - 1866 (1996)

Reduction of α-ketoesters bearing 5(N-methylbenzoylamino)-2,2,6,6-tetramethylheptan-3-ol as a chiral auxillary proceeds with high diastereoselectivity by using DIBAL as a reducing agent. The chiral auxiliary is recovered upon treatment with base, and α-hy

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