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CAS

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179927-01-6

Benzoic acid (1S,2S,6R)-6-acetoxy-2-bromo-4-methoxycarbonyl-cyclohex-3-enyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 179927-01-6 Structure

  • Basic information

    1. Product Name: Benzoic acid (1S,2S,6R)-6-acetoxy-2-bromo-4-methoxycarbonyl-cyclohex-3-enyl ester
    2. Synonyms: Benzoic acid (1S,2S,6R)-6-acetoxy-2-bromo-4-methoxycarbonyl-cyclohex-3-enyl ester
    3. CAS NO:179927-01-6
    4. Molecular Formula:
    5. Molecular Weight: 397.222
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 179927-01-6.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: Benzoic acid (1S,2S,6R)-6-acetoxy-2-bromo-4-methoxycarbonyl-cyclohex-3-enyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid (1S,2S,6R)-6-acetoxy-2-bromo-4-methoxycarbonyl-cyclohex-3-enyl ester(179927-01-6)
    11. EPA Substance Registry System: Benzoic acid (1S,2S,6R)-6-acetoxy-2-bromo-4-methoxycarbonyl-cyclohex-3-enyl ester(179927-01-6)

  • 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: 179927-01-6(Hazardous Substances Data)

179927-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 179927-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,9,2 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 179927-01:
(8*1)+(7*7)+(6*9)+(5*9)+(4*2)+(3*7)+(2*0)+(1*1)=186
186 % 10 = 6
So 179927-01-6 is a valid CAS Registry Number.

179927-01-6Upstream product

179927-01-6Downstream Products

179927-01-6Relevant articles and documents

The shikimate pathway. Part 8. Synthesis of (-)-3(R)-amino- 4(R),5(R)-dihydroxy-1-cyclohexene-1-carboxylic acid: The 3(R)- amino analogue of (-)-shikimic acid

Adams,Bailey,Brettle,Cross,Frederickson,Haslam,MacBeath,Davies

, p. 8565 - 8580 (1996)

The first successful method for the introduction of nitrogenous functionality at C-3 of the shikimate nucleus has been developed and has allowed the synthesis of (-)-3(R)-amino-4(R),5(R)- dihydroxy-1-cyclohexene-1-carboxylic acid [the 3(R)-amino analogue of (-)-shikimic acid] in seven steps from the parent acid.

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