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866467-71-2

(3S,7aR)-6-benzyl-7-methoxy-3-phenyltetrahydro-5H-imidazo[1,5-c][1,3]thiazol-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 866467-71-2 Structure

  • Basic information

    1. Product Name: (3S,7aR)-6-benzyl-7-methoxy-3-phenyltetrahydro-5H-imidazo[1,5-c][1,3]thiazol-5-one
    2. Synonyms: (3S,7aR)-6-benzyl-7-methoxy-3-phenyltetrahydro-5H-imidazo[1,5-c][1,3]thiazol-5-one
    3. CAS NO:866467-71-2
    4. Molecular Formula:
    5. Molecular Weight: 340.446
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 866467-71-2.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: (3S,7aR)-6-benzyl-7-methoxy-3-phenyltetrahydro-5H-imidazo[1,5-c][1,3]thiazol-5-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S,7aR)-6-benzyl-7-methoxy-3-phenyltetrahydro-5H-imidazo[1,5-c][1,3]thiazol-5-one(866467-71-2)
    11. EPA Substance Registry System: (3S,7aR)-6-benzyl-7-methoxy-3-phenyltetrahydro-5H-imidazo[1,5-c][1,3]thiazol-5-one(866467-71-2)

  • 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: 866467-71-2(Hazardous Substances Data)

866467-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 866467-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,4,6 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 866467-71:
(8*8)+(7*6)+(6*6)+(5*4)+(4*6)+(3*7)+(2*7)+(1*1)=222
222 % 10 = 2
So 866467-71-2 is a valid CAS Registry Number.

866467-71-2Relevant articles and documents

An unusual stereochemical outcome of radical cyclization: Synthesis of (+)-biotin

Chavan, Subhash P.,Chittiboyina, Amar G.,Ramakrishna, Guduru,Tejwani, Rajkumar B.,Ravindranathan,Kamat, Subhash K.,Rai, Beena,Sivadasan, Latha,Balakrishnan, Kamalam,Ramalingam,Deshpande

, p. 9273 - 9280 (2005)

An enantioselective synthesis of (+)-biotin 1 starting from naturally available cysteine is described. The key steps are the unusual stereochemical outcome of radical cyclization of compound 10 to prepare 5,5-fused system 11, and the introduction of C4-sidechain at C6 in 13 via a Grignard reaction.

7 - alkoxy -3 - phenyl tetrahydroimidazo [1,5 - c] thiazole -5 (1H) - method for preparing compound of

-

Paragraph 0045-0050; 0087-0088, (2020/02/10)

The invention discloses a preparation method of a 7-alkoxy-3-phenyltetrahydroimidazo[1,5-c]thiazole-5(1H)-one compound. The method comprises the following steps: sequentially reacting a dihydroimidazo[1,5-c]-thiazole-5,7(3H,6H)-dione compound with zinc po

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