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3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-1-phenyl-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103174-73-8

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103174-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103174-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,7 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 103174-73:
(8*1)+(7*0)+(6*3)+(5*1)+(4*7)+(3*4)+(2*7)+(1*3)=88
88 % 10 = 8
So 103174-73-8 is a valid CAS Registry Number.

103174-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name C5H2Me2(CO2Et)2NPh

1.2 Other means of identification

Product number -
Other names diethyl 1,4-dihydro-2,6-dimethyl-1-phenyl-3,5-pyridinedicarboxylate

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:103174-73-8 SDS

103174-73-8Downstream Products

103174-73-8Relevant academic research and scientific papers

ONE CARBON UNIT TRANSFER TO ENAMINES THROUGH OXAZOLLIDINES AND TETRAHYDRO-2H-1,3-OXAZINE

Singh, Harjit,Sarin, Rakesh,Singh, Kamaljit

, p. 3039 - 3042 (1986)

Oxazolidines and tetrahydro-2H-1,3-oxazine undergo acid catalysed transfer of C2 carbon unit inbetween two nucleophilic carbons of stabilised enamines.

CARBON TRANSFER REACTIONS WITH HETEROCYCLES-V. A FACILE SYNTHESIS OF NIFEDIPINE AND ANALOGUES

Singh, Harjit,Singh, Kamaljit

, p. 3967 - 3974 (2007/10/02)

Oxazolidines and tetrahydro-(2H)-1,3-oxazines transfer their C(2) units at the carbonyl group oxidation level to alkyl-β-amino/anilinocrotonates to form 1,4-dihydropyridines elaborated at C-4.

Synthesis and Properties of Ethyl 1,4-Dihydro-5-pyrimidinecarboxylates: Comparison of Dihydropyrimidines and Dihydropyridines

Kashima, Choji,Shimizu, Masao,Tagaya, Atsuko,Katoh, Akira,Omote, Yoshimori

, p. 901 - 919 (2007/10/02)

1,4-Dihydropyrimidines which have electron withdrowing groups were sythesized by the desulphurization of pyrimidine-4(1H)-thiones with Raney nickel.Since this compounds are the aza-analogues of dihydropyridines, comparisons of spectral data, pKa' values,

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