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2-Benzylphenylglycidylether is an organic compound with the chemical formula C16H15O2. It is a colorless to pale yellow liquid and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. 2-BENZYLPHENYLGLYCIDYLETHER is characterized by its ether linkage between a benzylphenyl group and a glycidyl group, which provides unique reactivity and properties. It is typically synthesized through the reaction of 2-benzylphenol with epichlorohydrin, and its applications span across various industries due to its versatility in chemical transformations.

2461-43-0

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2461-43-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2461-43-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2461-43:
(6*2)+(5*4)+(4*6)+(3*1)+(2*4)+(1*3)=70
70 % 10 = 0
So 2461-43-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O2/c1-2-6-13(7-3-1)10-14-8-4-5-9-16(14)18-12-15-11-17-15/h1-9,15H,10-12H2

2461-43-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-Benzylphenoxy)methyl]oxirane

1.2 Other means of identification

Product number -
Other names 2-Benzylphenyl glycidyl ether

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:2461-43-0 SDS

2461-43-0Downstream Products

2461-43-0Relevant academic research and scientific papers

Synthesis and plant growth retardant activity of bis-quaternary salts of ammonia from phenols

Sharma,Bala, Madhu

, p. 975 - 977 (2007/10/03)

Trialkylamines 3-(2-benzylphenoxy)-l-N,N-diethylaminpropan-2-ol (4a), 3-(4-benzylphenoxy)-l-N,N-diethylaminpropan-2-ol (4b), 3-(5-n-hutoxyphcnoxy)-l- N,N-diethylaminpropan-2-ol (4c) and 4,4'-bis(3-N,N-diethylamin-2- hydroxypropanoxy)biphenyl (9) were prepared from respective phenols and converted into corresponding bis-quaternary salts by reacting (4a-c) with malonyl chloride and (9) with ethyl bromide. These salts were tested for biological activity on germination, seedling growth and adventitious root formation on hypocotyl cuttings of Vigina radiata (SML-668). The results of biological studies of different compounds show that these salts do not inhibit seed germination and rather promotory in increasing shoot elongation if used from 10-50 μg/ml. However, all those compounds showed inhibitory action at higher concentration i.e. 100 μg/ml.

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