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1H-Benzimidazol-2-amine,4-chloro-(9CI) is a chemical compound belonging to the benzimidazole amine class, characterized by a molecular formula of C7H6ClN3. It features a heterocyclic aromatic structure with a chlorine atom at the 4-position on the benzimidazole ring, which may contribute to its potential applications in various fields such as pharmaceuticals, agrochemicals, and material science.

701-14-4

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701-14-4 Usage

Uses

Used in Pharmaceutical Industry:
1H-Benzimidazol-2-amine,4-chloro-(9CI) is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the benzimidazole ring and the chlorine atom, may provide specific biological activities or enhance the properties of the resulting pharmaceuticals, such as improving solubility, stability, or bioavailability.
Used in Agrochemical Industry:
In the agrochemical field, 1H-Benzimidazol-2-amine,4-chloro-(9CI) may be utilized as a building block for the development of new agrochemicals, such as pesticides or herbicides. Its chemical properties could contribute to the effectiveness of these products, potentially leading to improved crop protection and yield.
Used in Material Science:
1H-Benzimidazol-2-amine,4-chloro-(9CI) may also find applications in material science, where its unique structure could be employed to develop new materials with specific properties. For example, it could be used in the synthesis of advanced polymers, coatings, or other materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 701-14-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 701-14:
(5*7)+(4*0)+(3*1)+(2*1)+(1*4)=44
44 % 10 = 4
So 701-14-4 is a valid CAS Registry Number.

701-14-4 Well-known Company Product Price

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  • Aldrich

  • (761672)  2-Amino-7-chloro-1H-benzimidazole  95%

  • 701-14-4

  • 761672-500MG

  • 1,088.10CNY

  • Detail

701-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-1H-benzimidazol-2-amine

1.2 Other means of identification

Product number -
Other names 4-Chlor-2-amino-benzimidazol

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:701-14-4 SDS

701-14-4Downstream Products

701-14-4Relevant academic research and scientific papers

JAK-2 MODULATORS AND METHODS OF USE

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Page/Page column 213, (2008/06/13)

This invention relates to the field of protein tyrosine kinases and inhibitors thereof. In particular, the invention relates to inhibitors of JAK-2, pharmaceutical compositions of the compounds for inhibiting JAK-2, methods of inhibiting JAK-2 in a cell, comprising contacting a cell in which inhibition of JAK-2 is desired with a compound or pharmaceutical composition comprising a compound according to the invention. The also comprises methods of treating a disease or condition that involves JAK-2 comprising administering to a patient a pharmaceutical composition comprising a compound according to the invention

Method of inhibiting the advanced glycosylation of proteins using 1,2-disubstituted-benzimidazoles

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, (2008/06/13)

The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging). Accordingly, composition is disclosed which comprises 1,2-disubstituted benzimidazoles capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with the carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation. The method comprises contacting the target protein with the composition. Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.

Iminoisoindolinone metal complex

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, (2008/06/13)

Iminoisoindolinone metal complexes of formula STR1 wherein A represents a 5- or 6-membered heterocyclic radical which contains at least one further heteroatom and can be fused or doubled with benzene nuclei, M represents a divalent metal atom excluding the alkaline earth metals, X represents a hydrogen atom, Y represents a halogen atom, Z represents a nitro group, an alkoxycarbonyl group of 2 to 6 carbon atoms or a group of formula RY2 --, wherein R represents a hydrogen atom, an alkyl group of 1 to 6 carbon atoms which is substituted by an aryl radical or is unsubstituted, a cycloalkyl group of 5 to 6 carbon atoms, or represents an aryl group, and Y2 represents an oxygen or a sulphur atom, m and n are 0 to 4, p is 0 to 2, and the sum of m+n+p must be 4, which are useful for pigmenting high molecular organic material.

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