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Ethanone, 1-(1-methyl-1H-benzimidazol-2-yl)-, oxime (9CI) is a chemical compound with the molecular formula C10H11N2O. It is an oxime derivative of acetone, featuring a 1-methyl-1H-benzimidazol-2-yl group attached to the carbonyl carbon. Ethanone, 1-(1-methyl-1H-benzimidazol-2-yl)-, oxime (9CI) is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new molecules with biological activity. The oxime functional group in Ethanone, 1-(1-methyl-1H-benzimidazol-2-yl)-, oxime (9CI) can participate in various chemical reactions, making it a versatile intermediate in organic synthesis.

945-78-8

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945-78-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 945-78-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 945-78:
(5*9)+(4*4)+(3*5)+(2*7)+(1*8)=98
98 % 10 = 8
So 945-78-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3O/c1-7(12-14)10-11-8-5-3-4-6-9(8)13(10)2/h3-6,11H,1-2H3/b10-7-

945-78-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2Z)-3-methyl-2-(1-nitrosoethylidene)-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 1-Methyl-2-(1-oximino-aethyl)-benzimidazol

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:945-78-8 SDS

945-78-8Downstream Products

945-78-8Relevant academic research and scientific papers

Microwave-assisted synthesis of 2-substituted 4-biarylyl-1,3-thiazoles by carbon-carbon cross-coupling in water

Dawood, Kamal M.,El-Deftar, Moteaa M.

scheme or table, p. 1030 - 1038 (2010/06/16)

Suzuki-Miyaura and Heck-Mizoroki C-C cross-coupling reactions of 4-(halophenyl)-1,3-thiazoles with aryl(hetaryl)boronic acids or olefins, respectively, were investigated by using a catalytically active benzimidazole-based palladium(II) complex under both thermal and microwave heating conditions in water. The factors affecting the optimization of such reactions were evaluated.

Intramolecular Nitrogen-Phosphorus Interactions of Phosphate Esters

Bushey, Dean F.,Johnson, Brenda F.,Huang, Jamin

, p. 2091 - 2095 (2007/10/02)

Four different classes of phosphate esters derived from enols, phenols, carbinols, and oximes have been shown to undergo intramolecular rearrangements assisted by a neighboring nitrogen.The unexpected products from these rearrangements have been characterized by spectral methods, especially 13C NMR.Rearrangements involving the O-ethyl S-propyl thiophosphate group have led to particularly interesting results.

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