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CAS

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35607-83-1

(6R)-3-acetoxymethyl-8-oxo-7t-(2-thiophen-2-yl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 35607-83-1 Structure

  • Basic information

    1. Product Name: (6R)-3-acetoxymethyl-8-oxo-7t-(2-thiophen-2-yl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester
    2. Synonyms: (6R)-3-acetoxymethyl-8-oxo-7t-(2-thiophen-2-yl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester
    3. CAS NO:35607-83-1
    4. Molecular Formula:
    5. Molecular Weight: 562.667
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35607-83-1.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: (6R)-3-acetoxymethyl-8-oxo-7t-(2-thiophen-2-yl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (6R)-3-acetoxymethyl-8-oxo-7t-(2-thiophen-2-yl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester(35607-83-1)
    11. EPA Substance Registry System: (6R)-3-acetoxymethyl-8-oxo-7t-(2-thiophen-2-yl-acetylamino)-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester(35607-83-1)

  • 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: 35607-83-1(Hazardous Substances Data)

35607-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35607-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,0 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35607-83:
(7*3)+(6*5)+(5*6)+(4*0)+(3*7)+(2*8)+(1*3)=121
121 % 10 = 1
So 35607-83-1 is a valid CAS Registry Number.

35607-83-1Relevant articles and documents

An Extremely Powerful Acylation Reaction of Alcohols with Acid Anhydrides Catalyzed by Trimethylsilyl Trifluoromethanesulfonate

Procopiou, Panayiotis A.,Baugh, Simon P.D.,Flack, Stephen S.,Inglis, Graham G.A.

, p. 2342 - 2347 (2007/10/03)

Trimethylsilyl trifluoromethanesulfonate is an excellent catalyst for the acylation of alcohols with acid anhydrides. Highly functionalized primary, secondary, tertiary, and allylic alcohols, and phenols, were acylated cleanly and efficiently and in a fraction of the time used under the standard DMAP conditions.

2,4,6-TRIPYRIDINIO-1,3,5-TRIAZINE TRICHLORIDE, A NEW AND MILD ESTERIFICATION AGENT FOR PREPARATION OF PENICILLIN ESTERS

Murakami, Masayuki,Hajima, Makoto,Takami, Fumitaka,Yoshioka, Mitsuru

, p. 2055 - 2064 (2007/10/02)

Cyanuric chloride reacted with 3-molar equivalents of pyridine to give 2,4,6-tripyridinio-1,3,5-triazine trichloride, which was found to condense penicilins with alcohols under mild conditions to afford penicillin esters in good yields.Application to prep

CYCLOADDITION REACTIONS OF CEPHALOSPORIN COMPOUNDS, X. SYNTHESIS AND STEREOCHEMISTRY OF BENZHYDRYL 7β-(2-THIENYL)ACETAMIDO-2-SPIROCYCLOPROPYL-2(2',2'-DIPHENYL)-3-ACETOXYMETHYL-3-CEPHEM-4-CARBOXYLATE 1S(β)-OXIDE

Pitlik, Janos,Jaszberenyi, J. Csaba

, p. 847 - 854 (2007/10/02)

Cycloadditions are useful methods to synthesize novel β-lactam derivatives .In our laboratory we studied the 1,3-dipolar cycloaddition reactions of 2-methylenecephems with diazoalkanes .In this paper we report the synthesis and structure elucid

Process for preparing cephalosporin esters in the presence of liquid sulfur dioxide

-

, (2008/06/13)

A process for preparing a cephalosporin ester which comprises subjecting an organic halide or an alcohol to reaction with a cephalosporin acid, a cephalosporin acid halide or a salt thereof in the presence of liquid sulfur dioxide.

Extraction of N-blocked amino acids from aqueous media

-

, (2008/06/13)

N-blocked amino acids, particularly derived from natural sources such as fermentation liquors, are extractively esterified from aqueous media by treatment of the aqueous solution with a diazoalkane, e.g. diphenyldiazomethane, in the presence of a water-im

Process for the preparation of esters of N-blocked penicillin acids which comprises reacting the acid or a salt thereof with a primary amine and a nitrosating agent

-

, (2008/06/13)

A process is described for the preparation of esters of N-blocked amino acids (such as penicillins or cephalosporins) wherein the amino acid or a salt thereof is reacted with a primary amine and nitrosating agent.

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