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CAS

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1010702-05-2

(S)-2-(benzyloxycarbonylamino)-2-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)ethyl methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1010702-05-2 Structure

  • Basic information

    1. Product Name: (S)-2-(benzyloxycarbonylamino)-2-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)ethyl methanesulfonate
    2. Synonyms: (S)-2-(benzyloxycarbonylamino)-2-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)ethyl methanesulfonate
    3. CAS NO:1010702-05-2
    4. Molecular Formula:
    5. Molecular Weight: 373.427
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1010702-05-2.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: (S)-2-(benzyloxycarbonylamino)-2-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)ethyl methanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-(benzyloxycarbonylamino)-2-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)ethyl methanesulfonate(1010702-05-2)
    11. EPA Substance Registry System: (S)-2-(benzyloxycarbonylamino)-2-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)ethyl methanesulfonate(1010702-05-2)

  • 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: 1010702-05-2(Hazardous Substances Data)

1010702-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1010702-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,7,0 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1010702-05:
(9*1)+(8*0)+(7*1)+(6*0)+(5*7)+(4*0)+(3*2)+(2*0)+(1*5)=62
62 % 10 = 2
So 1010702-05-2 is a valid CAS Registry Number.

1010702-05-2Relevant articles and documents

ACYCLIC AMINE INHIBITORS OF NUCLEOSIDE PHOSPHORYLASES AND HYDROLASES

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Page/Page column 85; 86, (2008/06/13)

The invention relates to compounds of the general formula (I) which are inhibitors of purine nucleoside phosphorylases (PNPs) and/or nucleoside hydrolases (NHs). The invention also relates to the use of these compounds in the treatment of diseases and infections including cancer, bacterial infections, protozoal infections, and T-cell mediated disease and to pharmaceutical compositions containing the compounds.

(1S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2-hydroxyethylammonium benzoate, a versatile building block for chiral 2-aminoalkanols: Concise synthesis and application to nelfinavir, a potent HIV-protease inhibitor

Inaba, Takashi,Yamada, Yasuki,Abe, Hiroyuki,Sagawa, Shoichi,Cho, Hidetsura

, p. 1623 - 1628 (2007/10/03)

A concise synthesis of a versatile chiral C4 building block for 2- aminoalkanols, (1S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]2- hydroxyethylammonium benzoate (1a), was described. 1 (1a and its enantiomener 1b) acted as four stereoisomers of optically active 2-amino-1,3,4- butanetriol. The versatility of 1 was demonstrated by its application to the practical synthesis of nelfinavir (2), a potent HIV-protease inhibitor, as well as by the stereospecific synthesis of three diastereomers of 2.

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