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796882-45-6

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796882-45-6 Usage

General Description

1-((tert-Butoxycarbonyl)aMino)-2,2-difluorocyclopropanecarboxylic acid is a chemical compound with the molecular formula C11H15F2NO4. It is a cyclopropanecarboxylic acid derivative with a tert-butoxycarbonyl-protected amino group and two fluorine atoms attached to the cyclopropane ring. 1-((tert-Butoxycarbonyl)aMino)-2,2-difluorocyclopropanecarboxylic acid is commonly used as a building block in organic synthesis and medicinal chemistry. It has potential applications in the development of pharmaceuticals and agrochemicals due to its unique structural features. Notably, the tert-butoxycarbonyl group can be removed under mild conditions, making it a versatile intermediate for the preparation of various biologically active molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 796882-45-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,6,8,8 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 796882-45:
(8*7)+(7*9)+(6*6)+(5*8)+(4*8)+(3*2)+(2*4)+(1*5)=246
246 % 10 = 6
So 796882-45-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H13F2NO4/c1-7(2,3)16-6(15)12-8(5(13)14)4-9(8,10)11/h4H2,1-3H3,(H,12,15)(H,13,14)

796882-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-difluoro-1-[(2-methylpropan-2-yl)oxycarbonylamino]cyclopropane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-((tert-Butoxycarbonyl)amino)-2,2-difluorocyclopropanecarboxylic acid

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:796882-45-6 SDS

796882-45-6Downstream Products

796882-45-6Relevant articles and documents

Studies of 1-Amino-2,2-difluorocyclopropane-1-carboxylic Acid: Mechanism of Decomposition and Inhibition of 1-Aminocyclopropane-1-carboxylic Acid Deaminase

Liu, Cheng-Hao,Wang, Shao-An,Ruszczycky, Mark W.,Chen, Huawei,Li, Keqiang,Murakami, Kazuo,Liu, Hung-Wen

, p. 3342 - 3345 (2015)

1-Amino-2,2-difluorocyclopropane-1-carboxylic acid (DFACC) is of interest in the study of 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase due to the increased reactivity of its cyclopropyl functionality. It is shown that DFACC is unstable under near

Efficient synthesis of (R)- and (S)-1-amino-2,2-difluorocyclopropanecarboxylic acid via lipase-catalyzed desymmetrization of prochiral precursors

Kirihara, Masayuki,Kawasaki, Masashi,Takuwa, Tomofumi,Kakuda, Hiroko,Wakikawa, Takahiro,Takeuchi, Yoshio,Kirk, Kenneth L.

, p. 1753 - 1761 (2007/10/03)

The asymmetric syntheses of (+)-(R)-1-amino-2,2-difluorocyclopropane-1-carboxylic acid and its enantiomer have been accomplished. Key reactions in the synthetic design are lipase-catalyzed desymmetrization of a prochiral diol and a prochiral diacetate.

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