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Tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate is a chemical compound that is a derivative of benzimidazole. It is a carboxylate ester with a tert-butyl group, a chloromethyl group, and a benzimidazole ring. This versatile compound is known for its potential applications in various fields, particularly in organic chemistry, pharmaceuticals, and agrochemicals.

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  • 163798-87-6 Structure
  • Basic information

    1. Product Name: tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate
    2. Synonyms: tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate;1-(tert-Butoxycarbonyl)-2-(chloromethyl)-benzimidazole;tert-butyl 2-(chloroMethyl)-1H-benzo[d]iMidazole-1-carboxylate;1H-BenziMidazole-1-carboxylic acid, 2-(chloroMethyl)-, 1,1-diMethylethyl ester
    3. CAS NO:163798-87-6
    4. Molecular Formula: C13H15ClN2O2
    5. Molecular Weight: 266.7234
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 163798-87-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 377.6±44.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.23±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 2.01±0.10(Predicted)
    10. CAS DataBase Reference: tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate(163798-87-6)
    12. EPA Substance Registry System: tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate(163798-87-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 163798-87-6(Hazardous Substances Data)

163798-87-6 Usage

Uses

Used in Pharmaceutical Synthesis:
Tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure allows for the creation of a wide range of medicinal compounds.
Used in Agrochemical Production:
In the agrochemical industry, tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate is utilized as an intermediate in the production of various agrochemicals, contributing to the development of effective solutions for agricultural applications.
Used in Medicinal Chemistry Research:
Tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate is used as a research compound in medicinal chemistry, particularly for its potential as an anti-cancer agent. Its unique properties are being studied to explore its effectiveness in combating cancer cells.
Used in Organic Chemistry:
As a versatile compound in organic chemistry, tert-butyl 2-(chloromethyl)-1H-benzimidazole-1-carboxylate is employed in various chemical reactions and processes, showcasing its potential value in advancing the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 163798-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,7,9 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 163798-87:
(8*1)+(7*6)+(6*3)+(5*7)+(4*9)+(3*8)+(2*8)+(1*7)=186
186 % 10 = 6
So 163798-87-6 is a valid CAS Registry Number.

163798-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl 2-(chloromethyl)-1H-benzo[d]imidazole-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 2-(chloromethyl)benzimidazole-1-carboxylate

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:163798-87-6 SDS

163798-87-6Relevant articles and documents

Compositions of CXCR4 inhibitors and methods of preparation and use

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Page/Page column 76; 82, (2020/02/20)

The present invention provides compositions and methods of use for treating, preventing, or ameliorating a disease, disorder, or condition associated with a chemokine receptor such as CXCR4.

TRANSGLUTAMINASE 2 (TG2) INHIBITORS

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Paragraph 00335, (2020/03/02)

Described herein are compounds and pharmaceutical compositions containing such compounds which inhibit transglutaminase 2 (TG2). Also described herein are methods for using such TG2 inhibitors, alone or in combination with other compounds, for treating diseases or conditions that would benefit from TG2 inhibition.

Multi-substituted amine compound and its preparation and use (by machine translation)

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Paragraph 0187; 0188; 0210-0212; 0369; 0377-0379, (2018/04/27)

The invention belongs to the field of medical technology, in particular, the present invention provides the following formula I shown multi-substituted amine compound or its isomer or its pharmaceutically acceptable salt, ester, prodrug or hydrate, its pharmaceutical composition, preparation method thereof and its use in the preparation of medicine for treating aids in use. The compound or pharmaceutical composition containing the compound can be used as an inhibitor for inhibiting HIV integrase with LEDGF/p75 between protein - protein interaction and HIV integrase dimerization, then can be used for the treatment of aids. . (by machine translation)

NOVEL FERROPORTIN INHIBITORS

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Page/Page column 135, (2017/05/10)

The invention relates to novel ferroportin inhibitors of the general formula (I) pharmaceutical compositions comprising them and the use thereof as medicaments, in particular for the prophylaxis and/or treatment of diseases caused by a lack of hepcidin or iron metabolism disorders, such as particularly iron overload states such as in particular thalassemia and hemochromatosis.

PIPERIDINONES USEFUL IN THE TREATMENT OF INFLAMMATION

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Page/Page column 108, (2008/12/07)

There is provided compounds of formula (I): wherein R1, R2, R3, R4, R5, R6, R7, m and n have meanings given in the description, and pharmaceutically acceptable derivatives thereof, which compounds are useful in the treatment of diseases and conditions associated with inflammation.

AMD070, a CXCR4 chemokine receptor antagonist: Practical large-scale laboratory synthesis

Crawford, Jason B.,Chen, Gang,Gauthier, David,Wilson, Trevor,Carpenter, Bryon,Baird, Ian R.,McEachern, Ernie,Kaller, Alan,Harwig, Curtis,Atsma, Bem,Skerlj, Renato T.,Bridger, Gary J.

, p. 823 - 830 (2013/01/03)

An efficient and convergent four-step synthetic route to the CXCR4 chemokine receptor antagonist AMD070 (1) has been developed which employs only a single chromatographic step in the entire sequence. Novel reductive amination methods have been developed for the coupling of 2 and 3 in which a dehydrative imine formation is followed by reduction with an attenuated borohydride reagent (zinc chloride and sodium borohydride). Selective extraction methods were employed to purify synthetic intermediates and remove reagents and impurities. A procedure has also been developed to isolate 1 in a pure crystalline form.

CHEMOKINE RECEPTOR MODULATORS

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Page/Page column 216, (2008/12/08)

The invention provides compounds of Formula (I) and pharmaceutical composi tions comprising compounds of Formula (I). These compounds are useful treating or preventing HIV infections, and in treating proliferative disorders such as inhibiting the metastasis of various cancers

CHEMICAL COMPOUNDS

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Page/Page column 35, (2008/06/13)

The present invention provides compounds of Formula (I) comprising: including salts, solvates, and physiologically functional derivatives thereof, pharmaceutical formulations containing them, processes for their preparation, and methods of treatment using them.

Benzimidazole compounds and antiviral uses thereof

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, (2008/06/13)

The present invention relates to novel benzimidazole compounds that have useful antiviral activity. More specifically, the invention encompasses benzimidazole compounds that inhibit membrane fusion associated events such as viral transmission, reduce vira

Catechols as antimicrobial agents

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Page column 29, (2010/01/30)

Compounds, pharmaceutically acceptable salts, and compositions thereof of the general formula: wherein Ar is aryl and heteroaryl; R1, R2, R3, and R4are hydrido, alkyl, cyano, heteroaryl, hydroxy, amino, acylamino, halo, alkoxy, aryloxy, carboxyamido, alkenyl, cycloalkyl, heterocyclyl, acyl, acyloxy, carboalkoxy, carboxy, thio, sulfinyl, sulfonyl and sulfoxy, R5, R6, R7, and R8are hydrido and lower alkyl; and Het is a nitrogen-containing heterocyclic ring.

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