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CAS

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176640-18-9

(R)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 176640-18-9 Structure

  • Basic information

    1. Product Name: (R)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol
    2. Synonyms:
    3. CAS NO:176640-18-9
    4. Molecular Formula:
    5. Molecular Weight: 280.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 176640-18-9.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: (R)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol(176640-18-9)
    11. EPA Substance Registry System: (R)-3-Benzyloxy-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-butan-1-ol(176640-18-9)

  • 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: 176640-18-9(Hazardous Substances Data)

176640-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176640-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,6,4 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 176640-18:
(8*1)+(7*7)+(6*6)+(5*6)+(4*4)+(3*0)+(2*1)+(1*8)=149
149 % 10 = 9
So 176640-18-9 is a valid CAS Registry Number.

176640-18-9Relevant articles and documents

Design and synthesis of bisubstrate analogues for 3-hydroxy-3-methyl-glutaryl coenzyme A reductase

Taillefumier,De Fornel,Chapleur

, p. 615 - 618 (1996)

The coupling of metalated pyridine derivatives with a chiral Weinreb amide derived from gluconolactone followed by stereoselective reduction of the resulting ketone are the key steps of the synthesis of bisubstrates analogues of the HMGCoA reduction by HMGR.

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