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263351-43-5

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263351-43-5 Usage

Description

(3-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER, with the chemical formula C11H14INO2, is a white to off-white solid chemical compound. Derived from carbamic acid, it features a tert-butyl ester group that provides stability and ease of handling in laboratory environments. The iodo-benzyl group in its structure renders it valuable for specific organic synthesis applications. Due to its potentially harmful properties, it is crucial to handle this compound with care and appropriate safety measures.

Uses

Used in Organic Synthesis:
(3-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, particularly those involving the iodo-benzyl group, which can be a key component in the formation of new compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (3-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows it to be a building block for the development of new drugs, potentially contributing to the creation of medications with novel therapeutic properties.
Used in Chemical Research:
(3-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER is utilized as a research tool in chemical laboratories for studying reaction mechanisms and exploring new pathways in chemical synthesis. Its properties make it a valuable asset for scientists looking to understand and innovate within the field of organic chemistry.
Used in Material Science:
In material science, (3-IODO-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER may be employed in the development of new materials with specific properties. Its chemical structure could contribute to the creation of materials with unique characteristics, such as improved stability or reactivity, depending on the application.

Check Digit Verification of cas no

The CAS Registry Mumber 263351-43-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,3,5 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 263351-43:
(8*2)+(7*6)+(6*3)+(5*3)+(4*5)+(3*1)+(2*4)+(1*3)=125
125 % 10 = 5
So 263351-43-5 is a valid CAS Registry Number.

263351-43-5 Well-known Company Product Price

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  • Aldrich

  • (JWP00306)  (3-Iodo-benzyl)-carbamic acid tert-butyl ester  AldrichCPR

  • 263351-43-5

  • JWP00306-1G

  • 6,440.85CNY

  • Detail

263351-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[(3-iodophenyl)methyl]carbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,[(3-iodophenyl)methyl]-,1,1-dimethylethyl 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:263351-43-5 SDS

263351-43-5Relevant articles and documents

ADENINE DERIVATIVES AS PROTEIN KINASE INHIBITORS

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Page/Page column 130; 131, (2017/12/14)

The present invention relates to a compound suitable for use as a kinase inhibitor according to general formula (I) [compound (C), herein after], or the N- oxide, pharmaceutically acceptable salt, pharmaceutically acceptable solvate, or stereoisomer thereof, formula (I) wherein A, R1, R2, R3, R3', R4, R4', X, Y, Z, T are as defined in the claims. The invention further relates to an in vitro method of inhibiting protein kinase activity which comprises contacting a protein kinase with a compound of formula (I), or the N-oxide, pharmaceutically acceptable salt, pharmaceutically acceptable solvate, or stereoisomer thereof. The invention further relates to the compounds of formula (I) per se, as well as to their use as a medicament, and for use or in a method of treatment of a disease mediated by a protein kinase selected from cancer, inflammatory disorders, cardiovascular diseases, viral induced diseases, circulatory diseases, fibro-proliferative diseases and pain sensitization disorders.

NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS AND THE USES THEREOF

-

Paragraph 1332; 1333, (2013/07/25)

The invention relates to pyridinyl nicotinic acetylcholine receptor ligands, compositions comprising an effective amount of a pyridinyl nicotinic acetylcholine receptor ligand and methods to treat or prevent a condition, such as depression and nicotine dependence, comprising administering to an animal in need thereof an effective amount of a pyridinyl nicotinic acetylcholine receptor ligand.

Synthesis and application of a new fluorous-tagged ammonia equivalent

Nielsen, Simon D.,Smith, Garrick,Begtrup, Mikael,Kristensen, Jesper L.

supporting information; experimental part, p. 4557 - 4566 (2010/08/20)

A novel fluorous-tagged ammonia equivalent has been developed. It is based on a nitrogen-oxygen bond, which can be cleaved in a traceless manner by a molybdenum complex or samarium diiodide. The application in the synthesis of ureas, amides, sulfonamides, and carbamates is described. The scope of the fluo-rous N-O linker is exemplified by the synthesis of itopride, a drug used for the treatment of functional dyspepsia. Itopride was synthesized with the aid of fluorous purification methods and the product was isolated in good overall yield, with high purity.

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