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Naphthalene, 2-(methoxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42101-92-8

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42101-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42101-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,1,0 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42101-92:
(7*4)+(6*2)+(5*1)+(4*0)+(3*1)+(2*9)+(1*2)=68
68 % 10 = 8
So 42101-92-8 is a valid CAS Registry Number.

42101-92-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-naphthylmethyl methyl ether

1.2 Other means of identification

Product number -
Other names 2-(methoxymethyl)naphthalene

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:42101-92-8 SDS

42101-92-8Relevant academic research and scientific papers

Parallel mechanisms for the cycloaromatization of enyne allenes

Hughes, Thomas S.,Carpenter, Barry K.

, p. 2291 - 2298 (2007/10/03)

The Myers-Saito cycloaromatization of enyne allenes is proposed to consist of two parallel mechanisms, one involving a biradical and the other with dipolar character. MCSCF calculations suggest that a nonplanar cyclic allene could be fairly close in enthalpy to the biradical, while the planar zwitterion originally proposed as a possible second intermediate is in fact a transition state for the interconversion of the two enantiomeric cyclic allenes. Competitive trapping experiments rule out the presence of a single intermediate and are consistent with the participation of parallel pathways. The reaction of (Z)-hepta-1,2,4-trien-6-yne in cyclopentadiene gave an inseparable mixture of two tetracyclic products whose structures were elucidated with 2-D NMR.

Generation of Organic Cations from Group 14 Organometallic Compounds via Photoinduced Electron Transfer in the Presence of Cu(II) Salt

Mizuno, Kazuhiko,Yasueda, Masahiro,Otsuji, Yoshio

, p. 229 - 232 (2007/10/02)

Irradiations of acetonitrile-alcohol (3:1) solutions of arylmethyl silanes, germane, or stannanes in the presence of Cu(BF4)2 gave alkyl arylmethyl ethers in good yields via arylmethyl cations, The efficiency of this photoreaction increased in the order of Si- Ge- Sn-compounds.

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