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2-Propanol, 1,1-difluoro-1-[4-(2-methoxyethyl)phenoxy]-3-nitro-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192575-81-8

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192575-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192575-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,5,7 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 192575-81:
(8*1)+(7*9)+(6*2)+(5*5)+(4*7)+(3*5)+(2*8)+(1*1)=168
168 % 10 = 8
So 192575-81-8 is a valid CAS Registry Number.

192575-81-8SDS

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 (2S)-1,1-difluoro-1-[4-(2-methoxyethyl)phenoxy]-3-nitropropan-2-ol

1.2 Other means of identification

Product number -
Other names 2-Propanol,1,1-difluoro-1-[4-(2-methoxyethyl)phenoxy]-3-nitro-,(S)

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:192575-81-8 SDS

192575-81-8Downstream Products

192575-81-8Relevant academic research and scientific papers

Catalytic asymmetric nitroaldol reaction of α,α-difluoro aldehydes mediated by rare earth-lithium-BINOL complexes

Iseki, Katsuhiko,Oishi, Satoshi,Sasai, Hiroaki,Shibasaki, Masakatsu

, p. 9081 - 9084 (1996)

Rare earth-Li-BINOL complexes were used to catalyze nitroaldol reactions of α,α-difluoro aldehydes with nitromethane in a good enantioselective manner. The optical yields of nitroaldol 2a depend on the size of rare earth metals, and an Sm-Li-BINOL complex

Synthesis and biological evluation of a fluorinated analog of the β-adrenergic blocking agent, metoprolol

Iseki, Katsuhiko,Oishi, Satoshi,Sasai, Hiroaki,Shibasaki, Masakatsu

, p. 1273 - 1274 (2007/10/03)

Both enantiomers of a difluorinated metoprolol analog (1) were synthesized in enantiomerically pure form and evaluated as β-adrenergic blocking agents.

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