Cas 135038-13-0,((2S,5S,6R)-5-Acetoxy-6-acetoxymethyl-5,6-dihydro-2H-pyran-2-yloxy)-acetic acid benzyl ester

135038-13-0

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Basic information

Product Name: ((2S,5S,6R)-5-Acetoxy-6-acetoxymethyl-5,6-dihydro-2H-pyran-2-yloxy)-acetic acid benzyl ester
Synonyms:
CAS NO:135038-13-0
Molecular Formula:
Molecular Weight: 378.379
EINECS: N/A
Product Categories: N/A
Mol File: 135038-13-0.mol
Article Data: 2

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ((2S,5S,6R)-5-Acetoxy-6-acetoxymethyl-5,6-dihydro-2H-pyran-2-yloxy)-acetic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((2S,5S,6R)-5-Acetoxy-6-acetoxymethyl-5,6-dihydro-2H-pyran-2-yloxy)-acetic acid benzyl ester(135038-13-0)
EPA Substance Registry System: ((2S,5S,6R)-5-Acetoxy-6-acetoxymethyl-5,6-dihydro-2H-pyran-2-yloxy)-acetic acid benzyl ester(135038-13-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 135038-13-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135038-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,3 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 135038-13:
(8*1)+(7*3)+(6*5)+(5*0)+(4*3)+(3*8)+(2*1)+(1*3)=100
100 % 10 = 0
So 135038-13-0 is a valid CAS Registry Number.

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135038-13-0Relevant articles and documents

Asymmetric synthesis of anticancer β-lactams via Staudinger reaction: Utilization of chiral ketene from carbohydrate

Banik, Bimal K.,Banik, Indrani,Becker, Frederick F.

, p. 846 - 848 (2010)

We describe herein asymmetric synthesis of a novel anticancer β-lactam following Staudinger reaction with chiral carbohydrate as the ketene component with an achiral imine. The in vitro cytotoxicity studies of these β-lactams are also reported here.

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