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267432-03-1

C24H42N2O10Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 267432-03-1 Structure

  • Basic information

    1. Product Name: C24H42N2O10Si
    2. Synonyms: C24H42N2O10Si
    3. CAS NO:267432-03-1
    4. Molecular Formula:
    5. Molecular Weight: 546.69
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 267432-03-1.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: C24H42N2O10Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H42N2O10Si(267432-03-1)
    11. EPA Substance Registry System: C24H42N2O10Si(267432-03-1)

  • 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: 267432-03-1(Hazardous Substances Data)

267432-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 267432-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,7,4,3 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 267432-03:
(8*2)+(7*6)+(6*7)+(5*4)+(4*3)+(3*2)+(2*0)+(1*3)=141
141 % 10 = 1
So 267432-03-1 is a valid CAS Registry Number.

267432-03-1Relevant articles and documents

Amino acid fluoride for glycopeptide synthesis

Ito, Yukishige,Gerz, Manfred,Nakahara, Yoshiaki

, p. 1039 - 1042 (2000)

The formation of N-glycosidic linkage between N-acetylglucosamine (GlcNAc) and asparagine (Asn) was effected using aspartic acid γ-fluoride in combination with either glycosyl azide or silyl carbamate, by the action of Lindlar catalyst or Bu4NF. Further elongation of peptide chain was performed to give pentapeptide. This method was further applied into the synthesis of trisaccharidic asparagine, using p-methoxybenzyl assisted stereoselective β- mannosylation as the key transformation. (C) 2000 Elsevier Science Ltd.

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