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50846-36-1

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50846-36-1 Usage

General Description

2-Amino-2-methyl-propionitrile hydrochloride is a chemical compound with the molecular formula C4H9N2. It is a colorless to pale yellow liquid with a faint unpleasant odor and is soluble in water. 2-AMINO-2-METHYL-PROPIONITRILE HYDROCHLORIDE is commonly used as an intermediate in the production of various pharmaceuticals and agrochemicals. It is also utilized in organic synthesis as a building block for the preparation of other organic compounds. Additionally, 2-amino-2-methyl-propionitrile hydrochloride has the potential to be used as a reagent in the synthesis of new chemical entities for various applications in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 50846-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,4 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50846-36:
(7*5)+(6*0)+(5*8)+(4*4)+(3*6)+(2*3)+(1*6)=121
121 % 10 = 1
So 50846-36-1 is a valid CAS Registry Number.

50846-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-2-methylpropanenitrile hydrochloride

1.2 Other means of identification

Product number -
Other names 2-amino-2-methylpropanenitrile,hydrochloride

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:50846-36-1 SDS

50846-36-1Relevant articles and documents

Prebiotically Plausible Organocatalysts Enabling a Selective Photoredox α-Alkylation of Aldehydes on the Early Earth

Bechtel, Maximilian,Closs, Anna C.,Fuks, Elina,Trapp, Oliver

supporting information, (2020/08/17)

Organocatalysis is a powerful approach to extend and (enantio-) selectively modify molecular structures. Adapting this concept to the Early Earth scenario offers a promising solution to explain their evolution into a complex homochiral world. Herein, we present a class of imidazolidine-4-thione organocatalysts, easily accessible from simple molecules available on an Early Earth under highly plausible prebiotic reaction conditions. These imidazolidine-4-thiones are readily formed from mixtures of aldehydes or ketones in presence of ammonia, cyanides and hydrogen sulfide in high selectivity and distinct preference for individual compounds of the resulting catalyst library. These organocatalysts enable the enantioselective α-alkylation of aldehydes under prebiotic conditions and show activities that correlate with the selectivity of their formation. Furthermore, the crystallization of single catalysts as conglomerates opens the pathway for symmetry breaking.

CATHEPSIN INHIBITORS

-

Page/Page column 64-65, (2010/02/11)

This invention relates to a novel class of compounds, represented by the formula (I) below, wherein the meanings of R1, R2, R3 and R4 are indicated therein, which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis, osteoarthritis and rheumatoid arthritis.

Preparation of α-aminothioamides from aldehydes

Paventi, Martino,Edward, John T.

, p. 282 - 289 (2007/10/02)

The conversion of aldehydes into α-aminonitriles and thence into imidazolidin-4-thiones has been studied.Hydrolysis of the appropriate imidazolidin-4-thiones gave thioamides of nine naturally occuring α-amino acids.The possible pre-biotic significance of these compounds is discussed.

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