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118736-08-6

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118736-08-6 Usage

Uses

2-Methoxy-2-(2-naphthyl)acetonitrile (cas# 118736-08-6) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 118736-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,3 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 118736-08:
(8*1)+(7*1)+(6*8)+(5*7)+(4*3)+(3*6)+(2*0)+(1*8)=136
136 % 10 = 6
So 118736-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H11NO/c1-10(14-9-15)12-8-4-6-11-5-2-3-7-13(11)12/h2-8,10H,1H3/t10-/m0/s1

118736-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methoxy-2-(2-naphthyl)acetonitrile

1.2 Other means of identification

Product number -
Other names 2-Methoxy-2-(2-naphthyl)ethanenitrile

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:118736-08-6 SDS

118736-08-6Relevant articles and documents

Design, synthesis and evaluation of novel P450 fluorescent probes bearing α-cyanoether

Zhang, Rong,Kang, Kyung-Don,Shan, Guomin,Hammock, Bruce D.

, p. 4331 - 4334 (2003)

Four α-cyano-containing ethers based on 2-alkoxy-2-naphthylacetonitriles have been designed as a novel structural class of cytochrome P450 fluorescent probes. Their syntheses, fluorescence properties and evaluation in the fluorogenic assay of cytochrome P

A Sterically Congested α-Cyanoamine as a Cyanating Reagent: Cyanation of Acetals and Orthoesters

Kotani, Shunsuke,Sakamoto, Midori,Osakama, Kazuki,Nakajima, Makoto

supporting information, p. 6606 - 6609 (2015/10/29)

The cyanation of acetals and orthoesters by using a sterically congested α-cyanoamine as a cyanating reagent was investigated. The α-cyanoamine effectively facilitated cyanation in the presence of trichlorosilyl triflate to produce a variety of cyanated adducts in excellent yields. Analysis of the reaction mixture by 1H NMR spectroscopy revealed that trichlorosilyl triflate produced an oxocarbenium cation species as an intermediate.

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