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121282-70-0

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121282-70-0 Usage

Description

Boc-(+/-)-trans-2-aminocyclohexanol, also known as tert-Butyl (2-Hydroxycyclohexyl)carbamate, is an organic compound that serves as a crucial reagent in the synthesis of various chemical compounds. It is characterized by its ability to facilitate the conversion of nitro compounds into N-aryl acetamides, which are essential in the pharmaceutical and chemical industries.

Uses

Used in Pharmaceutical Industry:
Boc-(+/-)-trans-2-aminocyclohexanol is used as a synthetic reagent for the preparation of N-aryl acetamides from the corresponding nitro compounds. This application is significant because N-aryl acetamides are key intermediates in the synthesis of various pharmaceutical compounds, including those with analgesic, anti-inflammatory, and antimicrobial properties.
Used in Chemical Industry:
In the chemical industry, Boc-(+/-)-trans-2-aminocyclohexanol is utilized as a versatile reagent for the synthesis of a wide range of organic compounds. Its ability to convert nitro compounds into N-aryl acetamides makes it a valuable tool in the development of new materials and chemicals with diverse applications, such as in the fields of agriculture, plastics, and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 121282-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,2,8 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 121282-70:
(8*1)+(7*2)+(6*1)+(5*2)+(4*8)+(3*2)+(2*7)+(1*0)=90
90 % 10 = 0
So 121282-70-0 is a valid CAS Registry Number.

121282-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-(+/-)-trans-2-aminocyclohexanol

1.2 Other means of identification

Product number -
Other names trans-2-pyrrolidinocyclopentanol

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:121282-70-0 SDS

121282-70-0Relevant articles and documents

A new facile method for the chemoselective reductive transformation of azides to N-(tert-butoxycarbonyl)amines

Kotsuki, Hiyoshizo,Ohishi, Takeshi,Araki, Tomohiro

, p. 2129 - 2132 (1997)

A new chemoselective procedure for the reductive transformation of organic azides to the corresponding N-(tert-butoxycarbonyl)amino derivatives using triethylsilane and di-tert-butyl dicarbonate in the presence of a catalytic amount of 20% Degussa Pd(OH)

COMPOUNDS, COMPOSITIONS AND METHODS FOR SYNTHESIS

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Paragraph 001588; 001589; 001590; 001591; 00756; 00757; 0076, (2019/01/10)

The present disclosure, among other things, provides technologies for synthesis, including reagents and methods for stereoselective synthesis. In some embodiments, the present disclosure provides compounds useful as chiral auxiliaries. In some embodiments, the present disclosure provides reagents and methods for oligonucleotide synthesis. In some embodiments, the present disclosure provides reagents and methods for chirally controlled preparation of oligonucleotides. In some embodiments, technologies of the present disclosure are particularly useful for constructing challenging internucleotidic linkages, providing high yields and stereoselectivity.

CYCLOHEXANEDIAMINE COMPOUNDS AND METHODS FOR THEIR PREPARATION

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Paragraph 0112; 0113; 0114, (2014/10/04)

The present invention provides processes for the preparation of cyclohexanediamine compounds of formula Ia and intermediates thereof. The compounds are useful as Syk kinase inhibitors and in various pharmaceutical compositions, and particularly useful for treating conditions mediated at least in part by Syk kinase activity.

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