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1H-Naphth[1,2-e][1,3]oxazine, 2,3-dihydro-2-methyl- is a complex organic compound belonging to the class of naphthoxazines. It is characterized by a fused ring structure consisting of a naphthalene core and a 1,3-oxazine ring. The compound has a 2,3-dihydro configuration, indicating the presence of two hydrogen atoms in the 2 and 3 positions, and a methyl group attached at the 2 position. This specific arrangement of atoms and functional groups gives the compound unique chemical and physical properties, making it potentially useful in various applications such as pharmaceuticals, dyes, or other chemical industries.

35141-64-1

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35141-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35141-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,4 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35141-64:
(7*3)+(6*5)+(5*1)+(4*4)+(3*1)+(2*6)+(1*4)=91
91 % 10 = 1
So 35141-64-1 is a valid CAS Registry Number.

35141-64-1SDS

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-methyl-1,3-dihydrobenzo[f][1,3]benzoxazine

1.2 Other means of identification

Product number -
Other names HMS2620A18

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:35141-64-1 SDS

35141-64-1Relevant academic research and scientific papers

Oxidative ortho-amino-methylation of phenols via C-H and C-C bond cleavage

Sun, Wenbo,Lin, Huacan,Zhou, Wenyu,Li, Zigang

, p. 7491 - 7494 (2014/02/14)

Initiated by CCl3Br, phenols undergo efficient ortho-selective oxidative cross dehydrogenative coupling (CDC) with trimethylamine. When tetramethylethylenediamine (TMEDA) is used instead of trimethylamine, oxidative carbon-carbon activation coupling (CAC) could occur to give the same salicylamines together with CDC by-products. These reactions are accelerated by a gold salt.

Ligands for the Alkali Metals. Part 7. Synthesis and Characterisation of Crown Ether Macrocycles Containing the Di-1-naphthylmethyl Unit as a Novel Steric Barrier

Lockhart, Joyce C.,McDonnell, Martin B.,Tyson, Philip D.

, p. 2153 - 2160 (2007/10/02)

The first examples of crown ethers in which each end of the ether strand is fixed to one blade of a molecular propeller (a dinaphthylmethane) have been synthesised.The resultant steric barriers have been found to slow crown-flexing sufficiently for kinetic processes to be observed with 1H or 13C n.m.r. in the temperature range 200-270 K. vic-Coupling constants for the ethylene oxide segments at ambient temperature indicate a very low proportion of trans-conformer in the conformational mix.The crowns also complex with the alkali cations in solution.

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