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2-Benzyl-4-methylthiazole is an organic compound with the molecular formula C10H11NS. It is a colorless to pale yellow crystalline solid that is soluble in organic solvents. This chemical is characterized by a thiazole ring, which is a five-membered aromatic ring containing a sulfur atom and a nitrogen atom, with a benzyl group attached to the 2-position and a methyl group at the 4-position. 2-Benzyl-4-methylthiazole is used as a synthetic intermediate in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the fragrance industry due to its unique odor profile. The compound is typically synthesized through various chemical reactions, such as the condensation of appropriate precursors, and is subject to strict quality control measures to ensure its purity and stability.

7210-74-4

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7210-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7210-74-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7210-74:
(6*7)+(5*2)+(4*1)+(3*0)+(2*7)+(1*4)=74
74 % 10 = 4
So 7210-74-4 is a valid CAS Registry Number.

7210-74-4SDS

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-benzyl-4-methyl-thiazole

1.2 Other means of identification

Product number -
Other names 2-Benzyl-4-methyl-thiazole

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 -
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More Details:7210-74-4 SDS

7210-74-4Relevant academic research and scientific papers

Compatibility of Various Carbanion Nucleophiles with Heteroaromatic Nucleophilic Substitution by the SRN1 Mechanism

Wong, Jim-Wah,Natalie Jr., Kenneth J.,Nwokogu, Godson C.,Pisipati, Jyothi S.,Flaherty, Patrick T.,Greenwood, Thomas D.,Wolfe, James F.

, p. 6152 - 6159 (2007/10/03)

Carbanions generated from 2,4,4-trimethyl-2-oxazoline (1a), 2-benzyl-4,4-dimethyl-2-oxazoline (1b), 2,4-dimethylthiazole (13a), 2-benzyl-4-methylthiazole (13b), N,N-dimethylacetamide (17a), tert-butyl acetate (17b), ethyl phenylacetate (17c), N-methyl-N-phenyl-2-butenamide (22), tert-butyl 3-butenoate (25), and dimethyl methylphosphonate (29a) by means of KNH2 in liquid NH3 all reacted with 2-bromopyridine (2) via photoassisted reactions that exhibited characteristics of the SRN1 mechanism. Similar results were obtained in reactions of these carbanions with other substrates, including 2-chloroquinoline (6), iodobenzene (9), bromobenzene (10), and bromomesitylene (11).

Equilibrium acidities of 2-alkylthiazolium cations at the C-2α position

Bordwell,Satish,Jordan, Frank,Rios, Carlos B.,Chitong Chung

, p. 792 - 797 (2007/10/02)

The properties of the 2-(l-methoxyethyl)-3,4-dimethylthiazolium cation (3) and seven related thiazolium cations have been investigated as models for the behavior of 2-(l-hydroxyethyl)thiamin (1). The equilibrium acidity (pKHA +) of 3 in Me

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