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2-Butanol, 2-methyl-1-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22916-76-3

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22916-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22916-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,1 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22916-76:
(7*2)+(6*2)+(5*9)+(4*1)+(3*6)+(2*7)+(1*6)=113
113 % 10 = 3
So 22916-76-3 is a valid CAS Registry Number.

22916-76-3SDS

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 2-methyl-1-nitrobutan-2-ol

1.2 Other means of identification

Product number -
Other names 2-methyl-1-nitro-butan-2-ol

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:22916-76-3 SDS

22916-76-3Relevant academic research and scientific papers

P(RNCH2CH2)3N: An Efficient Promoter for the Nitroaldol (Henry) Reaction

Kisanga, Philip B.,Verkade, John G.

, p. 4298 - 4303 (2007/10/03)

The use of catalytic amounts of the proazaphosphatranes P(MeNCH2CH2)3N, P(i-PrNCH2CH2)3N and P(HNCH2CH2)(i-PrNCH2CH2) 2N as nonionic bases in the reaction of nitroalkanes with carbonyl compounds is reported. The reaction proceeds at room temperature in the presence of 2.2 equiv of magnesium sulfate to produce the corresponding β-nitroalkanols in generally superior yields. Aldehydes react quantitatively in 5-60 min, whereas ketones require up to 3 h to react with nitromethane and up to 7 h for the reaction of ketones with higher nitroalkanes.

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