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2-Thiophenecarboxylicacid,3-amino-4-cyano-5-methyl-,methylester(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85092-72-4

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85092-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85092-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,9 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85092-72:
(7*8)+(6*5)+(5*0)+(4*9)+(3*2)+(2*7)+(1*2)=144
144 % 10 = 4
So 85092-72-4 is a valid CAS Registry Number.

85092-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-amino-4-cyano-5-methylthiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names A-2279

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:85092-72-4 SDS

85092-72-4Downstream Products

85092-72-4Relevant academic research and scientific papers

Synthesis and fluorescence properties of aminocyanopyrrole and aminocyanothiophene esthers for biomedical and bioimaging applications

Agrebi, Asma,Allouche, Fatma,Alves, Sérgio,Baleiz?o, Carlos,Cherif, Oussama,Farinha, José Paulo

, (2020/03/11)

We prepared a series of substituted aminocyanopyrroles and another of aminocynaothiophenes. We describe an efficient new one-step synthetic strategy via the condensation of an alkyl sarcosinate and ethoxymethylenemalononitrile, through a Gewald-like reaction. The UV–visible absorption and steady-state and time resolved fluorescence properties of some representative compounds, as well as their acid-base behavior, is also presented. The compounds might be useful for medicinal applications and as bioimaging probes.

THIENOIMIDAZOLE DERIVATIVES, THEIR PRODUCTION AND USE

-

, (2008/06/13)

Benzimidazole derivatives of the formula (I): STR1 wherein the ring A is a thiophene ring which may optionally contain substitution in addition to the R 3 group; R 1 is hydrogen or an optionally substituted hydrocarbon residue which may be bonded through a heteroatom; R 2 and R 3 are independently a group capable of forming an anion or a group convertible thereinto; X is a direct bond or a spacer having an atomic length of two or less between the phenylene group and the phenyl group; and n is an integer of 1 or 2; or a salt thereof, have potent angiotensin II antagonistic activity and antihypertensive activity, thus being useful as therapeutic agents for treating circulatory system diseases such as hypertensive diseases, heart diseases (e.g. hypercardia, heart failure, cardiac infarction, etc.), strokes, cerebral apoplexy, nephritis, etc.

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