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CAS

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199388-20-0

3'S-(3,5-dimethoxyphenyl)-2'S-methyl-1-butanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 199388-20-0 Structure

  • Basic information

    1. Product Name: 3'S-(3,5-dimethoxyphenyl)-2'S-methyl-1-butanol
    2. Synonyms: 3'S-(3,5-dimethoxyphenyl)-2'S-methyl-1-butanol
    3. CAS NO:199388-20-0
    4. Molecular Formula:
    5. Molecular Weight: 224.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 199388-20-0.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: 3'S-(3,5-dimethoxyphenyl)-2'S-methyl-1-butanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3'S-(3,5-dimethoxyphenyl)-2'S-methyl-1-butanol(199388-20-0)
    11. EPA Substance Registry System: 3'S-(3,5-dimethoxyphenyl)-2'S-methyl-1-butanol(199388-20-0)

  • 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: 199388-20-0(Hazardous Substances Data)

199388-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199388-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,3,8 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 199388-20:
(8*1)+(7*9)+(6*9)+(5*3)+(4*8)+(3*8)+(2*2)+(1*0)=200
200 % 10 = 0
So 199388-20-0 is a valid CAS Registry Number.

199388-20-0Relevant articles and documents

Enantioselective synthesis and pharmacology of 11-hydroxy-(1'S,2'R)- dimethylheptyl]-Δ8-THC

Liddle, John,Huffman, John W.,Wiley, Jenny L.,Martin, Billy R.

, p. 2223 - 2226 (1998)

An enantioselective synthesis of the (1'S,2'R)-dimethylheptyl cannabinoid side chain has been developed and employed in the synthesis of 11-hydroxy-(1'S,2'R)-dimethylheptyl-Δ8-THC (3). Pharmacology, in vivo and in vitro, indicate (3) to be one of the most potent traditional cannabinoids known.

Enantioselective synthesis of 11-hydroxy-(1′S,2′R)-dimethylheptyl-Δ8-THC, a very potent CB1 agonist

Liddle, John,Huffman, John W

, p. 7607 - 7612 (2007/10/03)

An enantioselective synthesis of the (1S,2R)-dimethylheptyl cannabinoid side chain has been developed and employed in the synthesis of 11-hydroxy-(1′S,2′R)-dimethylheptyl-Δ8-THC, one of the most potent traditional cannabinoids known. The synthesis involves a highly stereoselective addition of dimethylcopperlithium to an enoyl sultam which incorporates Opplozer's auxiliary.

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