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116199-87-2

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116199-87-2 Usage

Description

3-Isopropenyl-2-oxo-1-benzimidazolinebutyric Acid Ethyl Ester, with the chemical name C16H19NO4 and CAS number 116199-87-2, is a yellow oil compound that plays a significant role in organic synthesis. Its unique chemical structure allows it to be a versatile building block for the creation of various organic compounds.

Uses

Used in Organic Synthesis:
3-Isopropenyl-2-oxo-1-benzimidazolinebutyric Acid Ethyl Ester is used as a synthetic intermediate for the production of various organic compounds. Its reactivity and functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Isopropenyl-2-oxo-1-benzimidazolinebutyric Acid Ethyl Ester is used as a key intermediate in the synthesis of drug molecules. Its unique structure can be incorporated into the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
3-Isopropenyl-2-oxo-1-benzimidazolinebutyric Acid Ethyl Ester is also utilized in the agrochemical industry as a precursor for the synthesis of pesticides and other crop protection agents. Its chemical properties enable the development of effective and targeted agrochemicals.
Used in Specialty Chemicals:
3-Isopropenyl-2-oxo-1-benzimidazolinebutyric Acid Ethyl Ester is employed in the production of specialty chemicals, such as dyes, pigments, and other performance-enhancing additives. Its versatility in organic synthesis allows for the creation of unique and innovative chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 116199-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,9 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 116199-87:
(8*1)+(7*1)+(6*6)+(5*1)+(4*9)+(3*9)+(2*8)+(1*7)=142
142 % 10 = 2
So 116199-87-2 is a valid CAS Registry Number.

116199-87-2SDS

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 ethyl 4-(2-oxo-3-prop-1-en-2-ylbenzimidazol-1-yl)butanoate

1.2 Other means of identification

Product number -
Other names 3-Isopropenyl-2-oxo-1-benzimidazolinebutyric Acid Ethyl Ester

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:116199-87-2 SDS

116199-87-2Relevant articles and documents

Synthesis of imidazobenzazepinthiones: A new series of HIV-1 reverse transcriptase inhibitors

Salaski, Edward J.

, p. 1387 - 1390 (1995)

A general route to a series of novel imidazobenzazepines that are 'carba' analogs of the TIBO class of non-nucleoside HIV-1 reverse transcriptase inhibitors has been developed. A pair of allyl side-chain containing compounds were found to have significant HIV-1 inhibitory activity.

HETEROCYCLIC COMPOUNDS USEFUL AS ANABOLIC AGENTS FOR LIVESTOCK ANIMALS

-

, (2008/06/13)

Compounds of formula (I) and pharmaceutically acceptable salts thereof are agonists at the beta-2 adrenoceptor. They are useful as feed additives for livestock animals.

Novel 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo[4,5,1-j-k][1]-benzazepin-2-(1H)-one

-

, (2008/06/13)

Novel 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo[4,5,l-j-k][1]-benzazepin-2-(1H)-one derivatives of the formula STR1 wherein R is selected from the group consisting of hydrogen, alkyl of 1 to 8 carbon atoms optionally substituted with a hydroxyl, aryl and aryloxy of 6 to 10 carbon atoms, cycloalkyl of 3 to 7 carbon atoms optionally interrupted with a heteroatom optionally substituted with alkyl of 1 to 4 carbon atoms and the wavy lines indicates that the 7-OH and 6-amino have the trans configuration and their non-toxic, pharmaceutically acceptable acid addition salts having remarkable anti-hypertensive and hypotensive activity and vasodilatatory activity and their preparation.

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