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CAS

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131380-41-1

L-arabino-Hept-1-enitol, 5,6-anhydro-1,2,3-trideoxy- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131380-41-1 Structure

  • Basic information

    1. Product Name: L-arabino-Hept-1-enitol, 5,6-anhydro-1,2,3-trideoxy- (9CI)
    2. Synonyms: L-arabino-Hept-1-enitol, 5,6-anhydro-1,2,3-trideoxy- (9CI)
    3. CAS NO:131380-41-1
    4. Molecular Formula: C7H12O3
    5. Molecular Weight: 144.16838
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131380-41-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: L-arabino-Hept-1-enitol, 5,6-anhydro-1,2,3-trideoxy- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-arabino-Hept-1-enitol, 5,6-anhydro-1,2,3-trideoxy- (9CI)(131380-41-1)
    11. EPA Substance Registry System: L-arabino-Hept-1-enitol, 5,6-anhydro-1,2,3-trideoxy- (9CI)(131380-41-1)

  • 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: 131380-41-1(Hazardous Substances Data)

131380-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131380-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,8 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131380-41:
(8*1)+(7*3)+(6*1)+(5*3)+(4*8)+(3*0)+(2*4)+(1*1)=91
91 % 10 = 1
So 131380-41-1 is a valid CAS Registry Number.

131380-41-1Downstream Products

131380-41-1Relevant articles and documents

A Stereochemically General Synthesis of 2-Deoxyhexoses via the Asymmetric Allylboration of 2,3-Epoxy Aldehydes

Roush, William R.,Straub, Julie A.,VanNieuwenhze, Michael S.

, p. 1636 - 1648 (2007/10/02)

A stereochemically general strategy for the synthesis of 2-deoxyhexoses is described.This new approach involves the asymmetric allylboration of epoxy aldehydes 12 and 13, prepared via the Sharpless asymmetric epoxidation reaction, as a means of establishi

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