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1992-08-1

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1992-08-1 Usage

Physical State

Colorless liquid

Odor

Faint, sweet

Uses

Solvent and reagent in various chemical reactions and processes; solvent in NMR spectroscopy; dissolution of a wide range of compounds, including polymers and proteins; production of fluorinated compounds; specialty solvent in organic synthesis; potential applications in drug delivery and as a cryoprotectant in biological samples.

Properties

Strong hydrogen bonding ability, versatile chemical, important in various industries (pharmaceuticals, biotechnology, and research).

Check Digit Verification of cas no

The CAS Registry Mumber 1992-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1992-08:
(6*1)+(5*9)+(4*9)+(3*2)+(2*0)+(1*8)=101
101 % 10 = 1
So 1992-08-1 is a valid CAS Registry Number.

1992-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-amino-4-methylphenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

1.2 Other means of identification

Product number -
Other names -

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:1992-08-1 SDS

1992-08-1Downstream Products

1992-08-1Relevant articles and documents

REACTIONS OF HIGHLY ELECTROPHILIC POLYFLUOROCARBONYL COMPOUNDS WITH PRIMARY ARYLAMINES

Chkanikov, N. D.,Sviridov, V. D.,Zelenin, A. E.,Galakhov, M. V.,Kolomiets, A. F.,Fokin, A. V.

, p. 323 - 328 (2007/10/02)

C-Hydroxyalkylation of primary arylamines by highly electrophilic polyfluorocarbonyl compounds results from the direct reaction of the initial reagents and is competitively inhibited by equilibrium N-hydroxyalkylation.The presence of steric hindrances to

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