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1-NITROETHANE-1,1-D2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13031-33-9

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13031-33-9 Usage

Uses

Nitroethane-1,1-d2 (CAS# 13031-33-9) is a useful isotopically labeled research compound.

Check Digit Verification of cas no

The CAS Registry Mumber 13031-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,3 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13031-33:
(7*1)+(6*3)+(5*0)+(4*3)+(3*1)+(2*3)+(1*3)=49
49 % 10 = 9
So 13031-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C2H5NO2/c1-2-3(4)5/h2H2,1H3/i2D2

13031-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dideuterio-1-nitroethane

1.2 Other means of identification

Product number -
Other names 1-Nitro-1,1-dideutero-ethan

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:13031-33-9 SDS

13031-33-9Relevant academic research and scientific papers

Organocatalytic Nitroaldol Reaction Associated with Deuterium-Labeling

Yamada, Tsuyoshi,Kuwata, Marina,Takakura, Ryoya,Monguchi, Yasunari,Sajiki, Hironao,Sawama, Yoshinari

supporting information, p. 637 - 641 (2017/12/13)

A deuterium-labeling reaction of nitroalkanes in deuterium oxide and the subsequent nitroaldol reaction have been accomplished under basic and organocatalytic conditions to provide the deuterium-labeled β-nitroalcohols in high yields and high deuterium contents. β-Deuterated β-nitroalcohols could be smoothly obtained from the reaction of nitroalkanes and various electrophiles using the easily-removal basic resin WA30. Furthermore, the asymmetric nitroaldol reaction using nitromethane and α-keto esters as electrophiles in the presence of a quinine-derived organocatalyst in deuterium oxide could provide the desired β-deuterated nitroalcohol derivatives with high enantioselectivities. (Figure presented.).

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