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74720-65-3

1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74720-65-3 Structure

  • Basic information

    1. Product Name: 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol
    2. Synonyms: 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol
    3. CAS NO:74720-65-3
    4. Molecular Formula:
    5. Molecular Weight: 263.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74720-65-3.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: 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol(74720-65-3)
    11. EPA Substance Registry System: 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-arabino-hex-1-enitol(74720-65-3)

  • 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: 74720-65-3(Hazardous Substances Data)

74720-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74720-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,2 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74720-65:
(7*7)+(6*4)+(5*7)+(4*2)+(3*0)+(2*6)+(1*5)=133
133 % 10 = 3
So 74720-65-3 is a valid CAS Registry Number.

74720-65-3Downstream Products

74720-65-3Relevant articles and documents

PREPARATION OF 4,6-O-BENZYLIDENE-2-C- AND -3-C-p-TOLYLSULFONYLHEX-2-ENOLPYRANOSIDE DERIVATIVES AND A 2-C-p-TOLYLSULFONYLHEX-2-ENITOL DERIVATIVE

Sakakibara, Tohru,Takai, Izumi,Yamamoto, Azuma,Tachimori, Yoshifusa,Sudoh, Rokuro,Ishido, Yoshiharu

, p. 189 - 200 (2007/10/02)

4,6-O-Benzylidenehex-2-enopyranoside derivatives having a 2-C- or 3-C-p-tolylsulfonyl group were synthesized from appropriate nitro sugars by the addition of p-toluenesulfinic acid followed by elimination of nitrous acid. 1,5-Anhydro-4,6-O-benzylidene-2,3

PREPARATION OF 4,6-O-BENZYLIDENE-3-DEOXY-3-C-NITRO-D-GLUCAL AND D-ALLAL AND 1,5-ANHYDRO-4,6-O-BENZYLIDENE-2,3-DIDEOXY-3-C-NITRO-D-threo-HEX-2-ENITOL

Sakakibara, Tohru,Nomura, Yutaka,Sudoh, Rokuro

, p. 53 - 62 (2007/10/02)

Oxidation of 1,5-anhydro-D-mannitol with sodium metaperiodate, followed by nitromethane cyclization and benzylidenation afforded 1,5-anhydro-3-nitrohexitol derivatives having the D-gluco, D-manno, and D-galacto configurations.Conversion of the nitro alcoh

Stereochemistry of Nucleophilic Addition Reactions. VIII. Preparation of 1,5-Anhydro-4,6-O-benzylidene-2,3-dideoxy-3-nitro-D-erythro-hex-2-enitol and Its Reactions with Some Nucleophiles

Sakakibara, Tohru,Nomura, Yutaka,Sudoh, Rokuro

, p. 1642 - 1646 (2007/10/02)

The title compound was synthesized from 1,5-anhydro-D-glucitol via nitromethane cyclization.The reduction of the compound with sodium borodeuteride afforded a mixture of saturated nitro compounds having an axial and equatorial deuterium atom at C-2 in an

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