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Cyclopropanecarboxylic acid, 2-nitro-, (1R,2R)-rel- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22882-43-5

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22882-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22882-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,8 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22882-43:
(7*2)+(6*2)+(5*8)+(4*8)+(3*2)+(2*4)+(1*3)=115
115 % 10 = 5
So 22882-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H5NO4/c6-4(7)2-1-3(2)5(8)9/h2-3H,1H2,(H,6,7)

22882-43-5SDS

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 rel-(1S,2S)-2-nitrocyclopropanecarboxylic acid

1.2 Other means of identification

Product number -
Other names 2-NITROCYCLOPROPANECARBOXYLIC 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:22882-43-5 SDS

22882-43-5Upstream product

22882-43-5Downstream Products

22882-43-5Relevant academic research and scientific papers

Multigram synthesis of trans -2-(trifluoromethyl)cyclopropanamine

Bezdudny, Andrii V.,Klukovsky, Denis,Simurova, Natalia,Mykhailiuk, Pavel K.,Shishkin, Oleg V.,Pustovit, Yurii M.

, p. 119 - 122 (2011)

2-(Trifluoromethyl)cyclopropanamine was synthesized. The key step of the synthesis is a transformation of the carboxy group into the trifluoromethyl group by using sulfur tetrafluoride. Twenty gram of the target product was conveniently prepared in a single batch. Georg Thieme Verlag Stuttgart · New York.

Synthesis of trans-(2-aminocyclopropyl)alanine - A key constituent of the novel antitumor antibiotic belactosin A

Brandl,Kozhushkov,Loscha,Kokoreva,Yufit,Howard,De Meijere

, p. 1741 - 1744 (2007/10/03)

Racemic 3-(trans-2-aminocyclopropyl)alanine was prepared in its 3,3-dideuterio-labelled form 3b from tert-butyl 2,3-dibromopropanoate 4 and nitromethane through a nine-step sequence in 8% overall yield. The newly developed access to enantiomerically pure (trans-2-nitrocyclopropyl)methanol (S,S)-6a also constitutes a formal synthesis of enantiomerically pure 3-(trans-2-aminocyclopropyl)alanine (S,S,S)-3a, a key intermediate for the total synthesis of the novel antitumor antibiotic belactosin A.

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