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(+/-)-occidentalol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 37574-03-1 Structure
  • Basic information

    1. Product Name: (+/-)-occidentalol
    2. Synonyms:
    3. CAS NO:37574-03-1
    4. Molecular Formula:
    5. Molecular Weight: 220.355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 37574-03-1.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: (+/-)-occidentalol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-occidentalol(37574-03-1)
    11. EPA Substance Registry System: (+/-)-occidentalol(37574-03-1)
  • 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: 37574-03-1(Hazardous Substances Data)

37574-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37574-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,7 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37574-03:
(7*3)+(6*7)+(5*5)+(4*7)+(3*4)+(2*0)+(1*3)=131
131 % 10 = 1
So 37574-03-1 is a valid CAS Registry Number.

37574-03-1Downstream Products

37574-03-1Relevant articles and documents

STEREOSELECTIVE SYNTHESYS OF (+/-)-OCCIDENTALOL

Mizuno, Yukio,Tomita, Masako,Irie, Hiroshi

, p. 107 - 110 (1980)

Stereoselective synthesis of the sesquiterpene alcohol, occidentalol starting from methyl c-4,c-9-dimethyl-6-methoxycarbonyl-2,7-dioxo-cis-decalyl-r-8-carboxylate was described.

Synthesis of Sesquiterpenes, Occidentalol, Chamaecynone and Related Compounds Characterised by a cis-Eudesmane Structure

Mizuno, Yukio,Mori, Reiko

, p. 2849 - 2854 (2007/10/02)

In continuation of our synthetic work for constructing the cis-decalin skeleton by a double Michael annulation using 3-methyl-4-methylenecyclohex-2-enone and its congeners with dimethyl 3-oxoglutarate, the sesquiterpenes, occidentalol, chamaecynone, and related compounds have been synthesised in a stereoselective manner.

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