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1374646-40-8

(S,E)-1-cyclohexyl-4-(3-nitrophenoxy)but-2-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1374646-40-8 Structure

  • Basic information

    1. Product Name: (S,E)-1-cyclohexyl-4-(3-nitrophenoxy)but-2-en-1-ol
    2. Synonyms: (S,E)-1-cyclohexyl-4-(3-nitrophenoxy)but-2-en-1-ol
    3. CAS NO:1374646-40-8
    4. Molecular Formula:
    5. Molecular Weight: 291.347
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1374646-40-8.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: (S,E)-1-cyclohexyl-4-(3-nitrophenoxy)but-2-en-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S,E)-1-cyclohexyl-4-(3-nitrophenoxy)but-2-en-1-ol(1374646-40-8)
    11. EPA Substance Registry System: (S,E)-1-cyclohexyl-4-(3-nitrophenoxy)but-2-en-1-ol(1374646-40-8)

  • 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: 1374646-40-8(Hazardous Substances Data)

1374646-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374646-40-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,6,4 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1374646-40:
(9*1)+(8*3)+(7*7)+(6*4)+(5*6)+(4*4)+(3*6)+(2*4)+(1*0)=178
178 % 10 = 8
So 1374646-40-8 is a valid CAS Registry Number.

1374646-40-8Relevant articles and documents

Iterative asymmetric allylic substitutions: Syn- and anti-1,2-diols through catalyst control

Park, Jin Kyoon,McQuade, D. Tyler

supporting information; experimental part, p. 2717 - 2721 (2012/04/17)

A copper-catalyzed asymmetric allylic boronation (AAB) gives access to syn- and anti-1,2-diols. The method facilitates an iterative strategy for the preparation of polyols (see scheme), such as the fully differentiated L-ribo-tetrol and protected D-arabin

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