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3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-[2-(trifluoromethyl)phenyl]-, 2-aminoethyl ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90105-80-9

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90105-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90105-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,0 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90105-80:
(7*9)+(6*0)+(5*1)+(4*0)+(3*5)+(2*8)+(1*0)=99
99 % 10 = 9
So 90105-80-9 is a valid CAS Registry Number.

90105-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminoethyl ethyl 2,6-dimethyl-4-(2-trifluoromethyl)phenyl-1,4-dihydropyridine-3,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names 3-(2-aminoethyl) 5-ethyl 1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)-pyridine-3,5-dicarboxylate

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:90105-80-9 SDS

90105-80-9Upstream product

90105-80-9Relevant academic research and scientific papers

Synthesis of diazipine and [3H]diazipine: Novel dihydropyridines as photoaffinity probes of calcium channels

Taki,Kuniyasu,Nakayama,Kanaoka

, p. 1860 - 1862 (1991)

Diazipine and [3H]diazipine were synthesized as new 1,4-dihydropyridine photoaffinity ligands containing a phenyldiazirine group. After simple high performance liquid chromatography separation, both compounds were purified in good overall yields. [3H]Diazipine (21.2 Ci/mmol) was synthesized in two steps from commercially available [3H]ethanolamine. Diazipine competitively inhibited [3H]PN200-110 binding to the calcium channel of cardiac membranes with high affinity.

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