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32350-46-2

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32350-46-2 Usage

General Description

(2Z)-4-(tert-butylamino)-4-oxobut-2-enoic acid, also known as N-tert-Butylglycine, is a chemical compound with the molecular formula C10H17NO3. It is an alpha-amino acid derivative, containing both a carboxylic acid group and an amino group, and is commonly used as a building block in the pharmaceutical industry for the synthesis of various compounds. This chemical is chiral, with the (2Z) designation indicating the geometry of the double bond in its structure. N-tert-Butylglycine has potential applications in the development of new drugs and as a precursor to other biologically active molecules. Additionally, it may also have some biological activity on its own, making it an interesting compound for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 32350-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,5 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32350-46:
(7*3)+(6*2)+(5*3)+(4*5)+(3*0)+(2*4)+(1*6)=82
82 % 10 = 2
So 32350-46-2 is a valid CAS Registry Number.

32350-46-2SDS

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 (Z)-4-(tert-butylamino)-4-oxobut-2-enoic acid

1.2 Other means of identification

Product number -
Other names T4158

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:32350-46-2 SDS

32350-46-2Relevant articles and documents

Terification of maleamic acids without double bond isomerization

Sanchez, Albert,Pedroso, Enrique,Grandas, Anna

experimental part, p. 2600 - 2606 (2010/09/07)

Activation of the carboxylic acid group of a maleamic acid by treatment with an arenesulfonyl chloride followed by addition of an alcohol affords a fumaramate or a maleamate, depending on the reaction conditions. The E isomer is obtained when the acid is treated with nearly equimolar amounts of 2,4,6-triisopropylbenzenesulfonyl chloride and an alcohol in pyridine. Replacement of pyridine by 2-picoline and use of a larger excess of activating agent (mesitylenesulfonyl chloride) and alcohol affords the Z isomer. In both cases, high diastereomeric excesses and yields are achieved.

Secondary aspartic acid amide esters

-

, (2008/06/13)

New secondary amines are described which are prepared from inexpensive, commercially available raw materials, are stable at room temperature, and are reactive toward electrophiles. The secondary amines are prepared by the addition of one or more primary amines with one or more male (amide/ester) and fumar (amide/ester) Michael receptors. The above amines can be used as coreactants with aliphatic polyisocyanates for polyurea coatings. The novel secondary amines are also described as particularly useful as part of a two-part liquid pavement marking composition for pavement markings.

[2+2]-cycloaddition of 'maleic isoimides' with ketenes and reactions of spiro-β-lactams to muconic and tetramic acids

Capraro,Winkler,Martin

, p. 362 - 378 (2007/10/02)

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