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594-39-8

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594-39-8 Usage

Description

TERT-AMYLAMINE is a chemical compound that is used as a substitute for the t-butylamino substituent in cyanobenzylamine derivatives. It is known for its unique properties and potential applications in various industries.

Uses

Used in Chemical Synthesis:
TERT-AMYLAMINE is used as a substitute for the t-butylamino substituent in cyanobenzylamine derivatives, which are important intermediates in the synthesis of various pharmaceuticals and agrochemicals. Its use as a substitute allows for the development of new compounds with improved properties and potential applications.
Used in Pharmaceutical Industry:
TERT-AMYLAMINE is used as a building block in the synthesis of various pharmaceutical compounds. Its unique properties and reactivity make it a valuable component in the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
TERT-AMYLAMINE is also used in the synthesis of agrochemicals, such as pesticides and herbicides. Its use as a substitute for the t-butylamino substituent in cyanobenzylamine derivatives allows for the development of new agrochemicals with enhanced performance and reduced environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 594-39-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 594-39:
(5*5)+(4*9)+(3*4)+(2*3)+(1*9)=88
88 % 10 = 8
So 594-39-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H13N/c1-4-5(2,3)6/h4,6H2,1-3H3/p+1

594-39-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (B24639)  tert-Pentylamine, 98%   

  • 594-39-8

  • 25g

  • 634.0CNY

  • Detail
  • Alfa Aesar

  • (B24639)  tert-Pentylamine, 98%   

  • 594-39-8

  • 100g

  • 2223.0CNY

  • Detail

594-39-8SDS

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-methylbutan-2-amine

1.2 Other means of identification

Product number -
Other names 1,1-Dimethyl-n-propylamine

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:594-39-8 SDS

594-39-8Relevant articles and documents

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Coleman,Yager

, p. 567 (1929)

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cis-2,5-dicyanopyrrolidine inhibitors of dipeptidyl peptidase IV: Synthesis and in vitro, in vivo, and x-ray crystallographic characterization

Wright, Stephen W.,Ammirati, Mark J.,Andrews, Kim M.,Brodeur, Anne M.,Danley, Dennis E.,Doran, Shawn D.,Lillquist, Jay S.,McClure, Lester D.,McPherson, R. Kirk,Orena, Stephen J.,Parker, Janice C.,Polivkova, Jana,Qiu, Xiayang,Soeller, Walter C.,Soglia, Carolyn B.,Treadway, Judith L.,VanVolkenburg, Maria A.,Wang, Hong,Wilder, Donald C.,Olson, Thanh V.

, p. 3068 - 3076 (2007/10/03)

Inhibitors of the glucagon-like peptide-1 (GLP-1) degrading enzyme dipeptidyl peptidase IV (DPP-IV) have been shown to be effective treatments for type 2 diabetes in animal models and in human subjects. A novel series of cis-2,5-dicyanopyrrolidine α-amino amides were synthesized and evaluated as inhibitors of dipeptidyl peptidase IV (DPP-IV) for the treatment of type 2 diabetes. 1-({[1-(Hydroxymethyl)cyclopentyl]amino}-acetyl)pyrrolidine-2,5-cis- dicarbonitrile (1c) is an achiral, slow-binding (time-dependent) inhibitor of DPP-IV that is selective for DPP-IV over other DPP isozymes and proline specific serine proteases, and which has oral bioavailability in preclinical species and in vivo efficacy in animal models. The mode of binding of the cis-2,5-dicyanopyrrolidine moiety was determined by X-ray crystallography. The hydrochloride salt of 1c was further profiled for development as a potential new treatment for type 2 diabetes.

Use of (S)-(Trifloxymethyl)oxirane in the synthesis of a chiral β-adrenoceptor antagonist, (R)- and (S)-9-[[3-(tert-butylamino)-2-hydroxypropyl]oximino]fluorene

Baldwin,McClure,Gross,Williams

, p. 931 - 936 (2007/10/02)

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