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323201-17-8

323201-17-8

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323201-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 323201-17-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,3,2,0 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 323201-17:
(8*3)+(7*2)+(6*3)+(5*2)+(4*0)+(3*1)+(2*1)+(1*7)=78
78 % 10 = 8
So 323201-17-8 is a valid CAS Registry Number.

323201-17-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-O-methyl 1-O-phenyl 3,6-dihydro-2H-pyridine-1,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names 3-methoxycarbonyl-1-phenoxycarbonyl-1,2,5,6-tetrahydropyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:323201-17-8 SDS

323201-17-8Relevant articles and documents

Synthesis of novel room temperature chiral ionic liquids. Application as reaction media for the Heck arylation of aza-endocyclic acrylates

Pastre, Julio C.,Ge?nisson, Yves,Saffon, Nathalie,Dandurand, Jany,Correia, Carlos R.D.

scheme or table, p. 821 - 836 (2010/09/10)

New achiral and chiral RTILs were prepared using novel and/or optimized synthetic routes. These new series of imidazolinium, imidazolium, pyridinium and nicotine-derived ionic liquids were fully characterized including differential scanning calorimetry (D

Selective fowler reductions: asymmetric total syntheses of isofagomine and other 1-azasugars from methyl nicotinate.

Zhao,Deo,Ganem

, p. 201 - 203 (2007/10/03)

[figure: see text] An efficient, high-yielding strategy has been developed for the asymmetric synthesis of 1-N-iminosugars (1-azasugars), a new class of glycosidase inhibitors with promising biomedical applications. A highly regioselective procedure for t

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