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Benzene, [(1S,2S)-2-nitro-1-(nitromethyl)butyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

921771-95-1

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921771-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 921771-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,1,7,7 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 921771-95:
(8*9)+(7*2)+(6*1)+(5*7)+(4*7)+(3*1)+(2*9)+(1*5)=181
181 % 10 = 1
So 921771-95-1 is a valid CAS Registry Number.

921771-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1S,2S)-2-nitro-1-(nitromethyl)butyl]benzene

1.2 Other means of identification

Product number -
Other names ((1S,2S)-2-Nitro-1-nitromethyl-butyl)-benzene

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:921771-95-1 SDS

921771-95-1Downstream Products

921771-95-1Relevant academic research and scientific papers

Asymmetric Michael addition of nitroalkanes to nitroalkenes catalyzed by C2-symmetric tridentate bis(oxazoline) and bis(thiazoline) zinc complexes

Lu, Shao-Feng,Du, Da-Ming,Xu, Jiaxi,Zhang, Shi-Wei

, p. 7418 - 7419 (2006)

The first asymmetric synthesis of 1,3-dinitro compounds through Michael addition of nitroalkanes to nitroalkenes catalyzed by C2-symmetric chiral tridentate bis(oxazoline) and bis(thiazoline) zinc complexes was achieved with high enantioselecti

Chiral squaramide-catalyzed highly diastereo- and enantioselective direct Michael addition of nitroalkanes to nitroalkenes

Yang, Wen,Du, Da-Ming

supporting information; experimental part, p. 12706 - 12708 (2012/01/06)

An efficient highly diastereo- and enantioselective direct Michael addition of nitroalkanes to nitroalkenes catalyzed by chiral squaramide catalyst has been developed. This organocatalytic reaction with a low catalyst loading (2 mol%) proceeded well to af

Highly diastereo- and enantioselective formal conjugate addition of nitroalkanes to nitroalkenes by chiral ammonium bifluoride catalysis

Ooi, Takashi,Takada, Saki,Doda, Kanae,Maruoka, Keiji

, p. 7606 - 7608 (2008/02/12)

(Chemical Equation Presented) A matter of control: A chiral quaternary ammonium bifluoride catalyst in combination with silyl nitronates results in the highly diastereo- and enantioselective formal conjugate addition of nitroalkanes to nitroalkenes (see s

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