Cas 271584-94-2,[(3aS,4S,6R,6aR)-2,2-Dimethyl-6-((E)-3-phenyl-allyloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-acetic acid methyl ester

271584-94-2

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Basic information

Product Name: [(3aS,4S,6R,6aR)-2,2-Dimethyl-6-((E)-3-phenyl-allyloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-acetic acid methyl ester
Synonyms:
CAS NO:271584-94-2
Molecular Formula:
Molecular Weight: 362.423
EINECS: N/A
Product Categories: N/A

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: [(3aS,4S,6R,6aR)-2,2-Dimethyl-6-((E)-3-phenyl-allyloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(3aS,4S,6R,6aR)-2,2-Dimethyl-6-((E)-3-phenyl-allyloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-acetic acid methyl ester(271584-94-2)
EPA Substance Registry System: [(3aS,4S,6R,6aR)-2,2-Dimethyl-6-((E)-3-phenyl-allyloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-acetic acid methyl ester(271584-94-2)

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: 271584-94-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 271584-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,1,5,8 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 271584-94:
(8*2)+(7*7)+(6*1)+(5*5)+(4*8)+(3*4)+(2*9)+(1*4)=162
162 % 10 = 2
So 271584-94-2 is a valid CAS Registry Number.

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271584-94-2Relevant academic research and scientific papers

Design and synthesis of mimics of S-Adenosyl-L-homocysteine as potential inhibitors of erythromycin methyltransferases

Hanessian, Stephen,Sgarbi, Paulo W.M.

, p. 433 - 437 (2007/10/03)

A series of indanotriazine C-ribosides were prepared as SAH mimics, and tested for their ability to inhibit erythromycin resistance methylases Erm AM and Erm C'. A carbocyclic analogue derived from quinic acid was also synthesized and tested. (C) 2000 Elsevier Science Ltd. All rights reserved.

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