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121195-03-7

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121195-03-7 Usage

Chemical Properties

Off-white solid

Check Digit Verification of cas no

The CAS Registry Mumber 121195-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,1,9 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 121195-03:
(8*1)+(7*2)+(6*1)+(5*1)+(4*9)+(3*5)+(2*0)+(1*3)=87
87 % 10 = 7
So 121195-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O2S/c1-2-14-10(13)8-6-7(11-12-8)9-4-3-5-15-9/h3-6H,2H2,1H3,(H,11,12)

121195-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-(Thiophen-2-yl)-1H-pyrazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 5-thiophen-2-yl-1H-pyrazole-3-carboxylate

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:121195-03-7 SDS

121195-03-7Downstream Products

121195-03-7Relevant articles and documents

The First Example of Azole-Fused Cyclic Anhydride Reacting in the Castagnoli-Cushman Way

Moreau, Ella,Dar'In, Dmitry,Krasavin, Mikhail

, p. 890 - 893 (2018)

Pyrazole-fused cyclic anhydrides have been employed for the first time as the Castagnoli-Cushman reaction partners to produce hitherto unknown 4-oxo-4,5,6,7-tetrahydropyrazolo[1,5- a ]pyrazine-7-carboxylates in remarkably convenient and speedy fashion. At

Synthesis of 3-aminomethyl-substituted pyrazoles and isoxazoles

Musatov,Starodubtseva,Rakishev,Turova,Vinogradov

experimental part, p. 1199 - 1203 (2011/12/15)

A series of new 3-(aminomethyl)pyrazoles and 3-(aminomethyl)isoxazoles was synthesized along a route involving the formation as key intermediates of esters of 5-substituted 1H-pyrazole-3-carboxylic and 1H-isoxazole-3-carboxylic acids. All compounds obtain

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