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N-allyl-N-(2-hydroxy-1-hydroxymethylbut-3-enyl)-4-methylbenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 870264-49-6 Structure
  • Basic information

    1. Product Name: N-allyl-N-(2-hydroxy-1-hydroxymethylbut-3-enyl)-4-methylbenzenesulfonamide
    2. Synonyms: N-allyl-N-(2-hydroxy-1-hydroxymethylbut-3-enyl)-4-methylbenzenesulfonamide
    3. CAS NO:870264-49-6
    4. Molecular Formula:
    5. Molecular Weight: 311.402
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 870264-49-6.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: N-allyl-N-(2-hydroxy-1-hydroxymethylbut-3-enyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-allyl-N-(2-hydroxy-1-hydroxymethylbut-3-enyl)-4-methylbenzenesulfonamide(870264-49-6)
    11. EPA Substance Registry System: N-allyl-N-(2-hydroxy-1-hydroxymethylbut-3-enyl)-4-methylbenzenesulfonamide(870264-49-6)
  • 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: 870264-49-6(Hazardous Substances Data)

870264-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 870264-49-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,2,6 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 870264-49:
(8*8)+(7*7)+(6*0)+(5*2)+(4*6)+(3*4)+(2*4)+(1*9)=176
176 % 10 = 6
So 870264-49-6 is a valid CAS Registry Number.

870264-49-6Relevant articles and documents

Efficient and stereodivergent synthesis of deoxyimino sugars

Hong, Bor-Cherng,Chen, Zhong-Yi,Nagarajan, Arumugam,Kottani, Rudresha,Chavan, Vishal,Chen, Wei-Hung,Jiang, Yea-Fen,Zhang, Shuo-Cang,Liao, Ju-Hsiou,Sarshar, Sepehr

, p. 2457 - 2468 (2005)

Both cis- and trans-2-substituted-1,2,3,6-tetrahydro-pyridin-3-ols have been prepared via an aldol condensation-ring-closing metathesis sequence. A stereodivergent synthesis of optionally functionalized deoxyimino sugars was achieved via asymmetric dihydroxylation or epoxidation/nucleophilic substitution of these tetrahydropyridines.

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