436091-31-5 Usage
Description
4-(1H-Benzimidazol-1-yl)butanoic acid is a chemical compound that belongs to the category of benzimidazole derivatives. It is composed of a butanoic acid molecule with a benzimidazole ring attached to the fourth position. This chemical is characterized by its structural versatility and pharmacological properties, making it a valuable building block in the synthesis of various pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
4-(1H-Benzimidazol-1-yl)butanoic acid is used as a building block for the synthesis of various pharmaceuticals. Its carboxylic acid group allows for the creation of ester, amide, and other organic compounds, which can be utilized in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 4-(1H-Benzimidazol-1-yl)butanoic acid is also used as a building block for the synthesis of various agrochemicals. Its structural versatility and pharmacological properties make it a promising candidate for the development of new agrochemicals with improved efficacy and selectivity.
Overall, 4-(1H-Benzimidazol-1-yl)butanoic acid's potential applications in both the pharmaceutical and agrochemical industries highlight its importance as a versatile chemical compound with a wide range of uses.
Check Digit Verification of cas no
The CAS Registry Mumber 436091-31-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,0,9 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 436091-31:
(8*4)+(7*3)+(6*6)+(5*0)+(4*9)+(3*1)+(2*3)+(1*1)=135
135 % 10 = 5
So 436091-31-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O2/c14-11(15)6-3-7-13-8-12-9-4-1-2-5-10(9)13/h1-2,4-5,8H,3,6-7H2,(H,14,15)
436091-31-5Relevant articles and documents
Barton esters for initiator-free radical cyclisation with heteroaromatic substitution
Coyle, Robert,Fahey, Karen,Aldabbagh, Fawaz
, p. 1672 - 1682 (2013/03/28)
S-(1-Oxido-2-pyridinyl)-1,1,3,3-tetramethylthiouronium hexafluorophosphate (HOTT) facilitates the first examples of efficient radical cyclisation with (hetero)aromatic substitution via Barton ester intermediates. Cyclopropyl and alkyl radicals allow acces
Octahydro-2H-pyrido[1,2-a] pyrazine compounds
-
, (2008/06/13)
A compound selected from those of formula (I): 1wherein: Ra represents linear or branched (C1-C6)alkylene, X represents a group selected from W1, —C(W1)—W2—, —W2—C(W1)—, —W2—C(W1)W2—, —W2-Ra- and —CH(OR1)— wherein W1, W2 and R1 are as defined in the description, when Y represents aryl or heteroaryl, or X represents a group selected from single bond, —C(W1)—, —W2—C(W1)—, —W2-Ra and —CH(OR1)— wherein W1, W2, Ra and R1 are as defined hereinbefore, when Y represents a fused bicyclic group, of formula: 2?wherein: A represents nitrogen-containing heterocycle having from 4 to 7 ring members that is unsaturated or partially saturated and optionally contains a second hetero atom, B represents phenyl ring optionally substituted by one or more groups as defined in the description, its isomers, and addition salts thereof with a pharmaceutically acceptable acid or base, medicinal products containing the same are useful in the treatment of cognitive deficiencies.
