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1H-Imidazole-2-methanol, 4-nitro-alpha-(trifluoromethyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105480-33-9

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105480-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105480-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,8 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105480-33:
(8*1)+(7*0)+(6*5)+(5*4)+(4*8)+(3*0)+(2*3)+(1*3)=99
99 % 10 = 9
So 105480-33-9 is a valid CAS Registry Number.

105480-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-1-(5-nitro-1H-imidazol-2-yl)ethanol

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:105480-33-9 SDS

105480-33-9Downstream Products

105480-33-9Relevant academic research and scientific papers

THERMAL CONDENSATION OF IMIDAZOLE WITH TRIFLUOROACETALDEHYDE

Fujii, Shozo,Maki, Yasuo,Kimoto, Hiroshi,Cohen, Louis A.

, p. 415 - 428 (1985)

The title condensation occurred readily at reflux (100 deg C) with the methyl hemiacetal of trifluoroacetaldehyde and provided 37.3percent of 4(5)-(1'-hydroxy-2',2',2'-trifluoroethyl)-imidazole as the major product, together with 8.8percent of 2-(1'-hydroxy-2',2',2'-trifluoroethyl)imidazole, 7.2percent of 2,4(5)-bis-(1'-hydroxy-2',2',2',-trifluoroethyl)imidazole and 0.4percent of the 4,5-bis-product. (Trifluoroacetyl)imidazoles were prepared by oxidation of these condensation products.Nitration and bromination of the condensation products gave the corresponding nitro- and bromoimidazoles, respectively.

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