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115890-33-0

3-azido-4-O-benzyl-3-deoxy-1,2-O-isopropylidene-D-erythritol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115890-33-0 Structure

  • Basic information

    1. Product Name: 3-azido-4-O-benzyl-3-deoxy-1,2-O-isopropylidene-D-erythritol
    2. Synonyms: 3-azido-4-O-benzyl-3-deoxy-1,2-O-isopropylidene-D-erythritol
    3. CAS NO:115890-33-0
    4. Molecular Formula:
    5. Molecular Weight: 277.323
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115890-33-0.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: 3-azido-4-O-benzyl-3-deoxy-1,2-O-isopropylidene-D-erythritol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-azido-4-O-benzyl-3-deoxy-1,2-O-isopropylidene-D-erythritol(115890-33-0)
    11. EPA Substance Registry System: 3-azido-4-O-benzyl-3-deoxy-1,2-O-isopropylidene-D-erythritol(115890-33-0)

  • 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: 115890-33-0(Hazardous Substances Data)

115890-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115890-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,9 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115890-33:
(8*1)+(7*1)+(6*5)+(5*8)+(4*9)+(3*0)+(2*3)+(1*3)=130
130 % 10 = 0
So 115890-33-0 is a valid CAS Registry Number.

115890-33-0Relevant articles and documents

Origins of the double asymmetric induction on proline-catalyzed aldol reactions

Calderon, Felix,Doyagueez, Elisa G.,Cheong, Paul Ha-Yeon,Fernandez-Mayoralas, Alfonso,Houk

supporting information; experimental part, p. 7916 - 7920 (2009/04/11)

(Chemical Equation Presented) Computational studies to elucidate the origin of the double asymmetric induction on proline-catalyzed aldol reaction have been performed using HF/6-31G(d) calculations. The computed transition structures explain the experimen

Synthesis of the 1,4-diazepan-2-one moiety of liposidomycins

Kim, Kwan Soo,Cho, In Haeng,Ahn, Yeong Hee,Park, Jong Ii

, p. 1783 - 1786 (2007/10/02)

The two stereoisomers 12 and 16 of 1,4-dimethyl-1,4-diazepan-2-one, a central feature of liposidomycins, have been synthesized starting from L-ascorbic acid and sarcosine.

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