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114772-25-7

114772-25-7

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114772-25-7 Usage

Description

2-BUTYL-1H-IMIDAZOLE-4,5-DICARBONITRILE, also known as BIC, is a white to off-white crystalline solid that belongs to the imidazole family and contains two butyl groups. It is a chemical compound that is sparingly soluble in water but more soluble in organic solvents. Classified as a nitrile, BIC contains a cyano group (-CN) and is known for its potential toxicological effects, necessitating careful handling and adherence to proper safety protocols.

Uses

Used in Pharmaceutical Industry:
2-BUTYL-1H-IMIDAZOLE-4,5-DICARBONITRILE is used as a key intermediate in the synthesis of various drugs, including potential anticancer and antifungal compounds. Its unique chemical structure allows for the development of new therapeutic agents that can target specific biological pathways.
Used in Agrochemical Production:
In the agrochemical industry, 2-BUTYL-1H-IMIDAZOLE-4,5-DICARBONITRILE serves as a building block in the production of various agrochemicals. Its properties enable the creation of compounds that can be used to protect crops from pests and diseases, thereby increasing agricultural productivity.
Used in Specialty Chemicals Production:
2-BUTYL-1H-IMIDAZOLE-4,5-DICARBONITRILE is also utilized in the production of specialty chemicals, where its unique properties can be harnessed for specific applications in various industries. Its versatility as a chemical intermediate makes it valuable in the synthesis of compounds for use in areas such as materials science, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 114772-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,7 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114772-25:
(8*1)+(7*1)+(6*4)+(5*7)+(4*7)+(3*2)+(2*2)+(1*5)=117
117 % 10 = 7
So 114772-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N4/c1-2-3-4-9-12-7(5-10)8(6-11)13-9/h2-4H2,1H3,(H,12,13)

114772-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Butyl-1H-imidazole-4,5-dicarbonitrile

1.2 Other means of identification

Product number -
Other names butylimidazoledicarbonitrile

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:114772-25-7 SDS

114772-25-7Relevant articles and documents

ANGIOTENSIN II ANTAGONIST 1-BIPHENYLMETHYLIMIDAZOLE COMPOUNDS AND THEIR THERAPEUTIC USE

-

, (2008/06/13)

Compounds of the following formula (I) or the formula (I) p : STR1 wherein R 1 is alkyl or alkenyl; R 2 and R 3 are hydrogen, alkyl, alkenyl, cycloalkyl, aralkyl, aryl, or aryl fused to cycloalkyl; R 4 is hydrogen, alkyl, alkanoyl, alkenoyl, arylcarbonyl, alkoxycarbonyl, tetrahydropyranyl, tetrahydrothiopyranyl, tetrahydrothienyl, tetrahydrofuryl, a group of formula--SiR a R b R c, in which R a, R b and R c are alkyl or aryl, alkoxymethyl, (alkoxyalkoxy)methyl, haloalkoxymethyl, aralkyl, aryl or alkanoyloxymethoxycarbonyl; R 5 is carboxy or--CONR 8 R 9, wherein R 8 and R 9 hydrogens or alkyl, or R 8 and R 9 together form alkylene; R 6 is hydrogen, alkyl, alkoxy or halogen; R. sup.7 is carboxy or tetrazol-5-yl; R p. sup.1 is hydrogen, alkyl, cycloalkyl or alkanoyl; R p 2 is a single bond, alkylene or alkylidene; R p 3 and R p 4 are each hydrogen or alkyl; R. sub.p 6 is carboxy or tetrazol-5-yl; and X p is oxygen or sulfur; and pharmaceutically acceptable salts and esters thereof. The compounds are AII receptor antagonists and thus have hypotensive activity and can be used for the treatment and prophylaxis of hypertension. The compounds may be prepared by reacting a biphenylmethyl compound with an imidazole compound.

ANGIOTENSIN II RECEPTOR BLOCKING IMIDAZOLES

-

, (2008/06/13)

Substituted imidazoles such as STR1 are useful as angiotensin II blockers. These compounds have activity in treating hypertension and congestive heart failure.

Stable Tellurium Ylides: Synthesis and Reactivity of Diorganyltelluronium 4,5-Dicyanoimidazol-2-ylides

Tappeiner, Guenther,Bildstein, Benno,Sladky, Fritz

, p. 699 - 705 (2007/10/02)

Diorganyl tellurides R2Te (R = Me, Me3SiCH2, Ph) react with 2-diazo-4,5-dicyano-2H-imidazole (1) at -30 deg C to form the title compounds 2-4.The ylides 3 and 4 are thermally stable up to their melting points of 159 and 243 deg C, resp., whereas 2 undergoes a modified Steven rearrangement at 190 deg C with formation of a 2-(methyltelluro)imidazole (10).The reactivity of 2-4 is determined by an extreme charge separation between the onium centre and the ylide entity.No Wittig reactivity is observed, alkylation occurs at the imidazole nitrogen and carbanions lead to tetraorganyl tellurium compounds with limited stability.

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