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1H-Imidazol-4-ol, 4,5-dihydro-5,5-dimethyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90859-31-7

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90859-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90859-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,5 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90859-31:
(7*9)+(6*0)+(5*8)+(4*5)+(3*9)+(2*3)+(1*1)=157
157 % 10 = 7
So 90859-31-7 is a valid CAS Registry Number.

90859-31-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dimethyl-2-phenyl-1,4-dihydroimidazol-4-ol

1.2 Other means of identification

Product number -
Other names 1H-Imidazol-4-ol,4,5-dihydro-5,5-dimethyl-2-phenyl

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:90859-31-7 SDS

90859-31-7Downstream Products

90859-31-7Relevant academic research and scientific papers

Synthesis and Properties of 4H-Imidazoles

Casey, Michael,Moody, Christopher,Rees, Charles W.

, p. 1389 - 1394 (2007/10/02)

The photolysis of 1-vinyltetrazoles to give 1H-imidazoles is extended to the synthesis of isolable nonaromatic 4H-imidazoles when the vinyl group is terminally disubstituted.Thus photolysis of the 2-phenyltetrazole (7a), prepared from isobutyraldehyde, at

Synthesis and Properties of 4H-Imidazoles

Casey, Michael,Moody, Christopher J.,Rees, Charles W.

, p. 1082 - 1083 (2007/10/02)

Photolysis of alkenyltetrazoles (1) provides the first rational route to simple 4H-imidazoles (2); when unsubstituted at C-5 these are highly reactive towards nucleophiles and rearrange rapidly to the aromatic 1H-imidazoles on heating.

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