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CAS

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909023-11-6

(1S,2R)-3-(tert-Butyl-dimethyl-silanyloxy)-1-(4-methoxy-phenyl)-1-nitro-propan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 909023-11-6 Structure

  • Basic information

    1. Product Name: (1S,2R)-3-(tert-Butyl-dimethyl-silanyloxy)-1-(4-methoxy-phenyl)-1-nitro-propan-2-ol
    2. Synonyms:
    3. CAS NO:909023-11-6
    4. Molecular Formula:
    5. Molecular Weight: 341.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 909023-11-6.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: (1S,2R)-3-(tert-Butyl-dimethyl-silanyloxy)-1-(4-methoxy-phenyl)-1-nitro-propan-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,2R)-3-(tert-Butyl-dimethyl-silanyloxy)-1-(4-methoxy-phenyl)-1-nitro-propan-2-ol(909023-11-6)
    11. EPA Substance Registry System: (1S,2R)-3-(tert-Butyl-dimethyl-silanyloxy)-1-(4-methoxy-phenyl)-1-nitro-propan-2-ol(909023-11-6)

  • 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: 909023-11-6(Hazardous Substances Data)

909023-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 909023-11-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,0,2 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 909023-11:
(8*9)+(7*0)+(6*9)+(5*0)+(4*2)+(3*3)+(2*1)+(1*1)=146
146 % 10 = 6
So 909023-11-6 is a valid CAS Registry Number.

909023-11-6Relevant articles and documents

Diastereoselective and enantioselective Henry (nitroaldol) reaction utilizing a guanidine-thiourea bifunctional organocatalyst

Sohtome, Yoshihiro,Hashimoto, Yuichi,Nagasawa, Kazuo

, p. 2894 - 2897 (2006)

A highly enantio- and diastereoselective Henry reaction of various aldehydes with nitroethane was developed using the guanidine-thiourea bifunctional catalyst 1 (syn selectivity of 86:14 to 99:1 with 84-99% ee). A variety of nitroalkanes was treated with

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