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67741-16-6

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67741-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67741-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,4 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67741-16:
(7*6)+(6*7)+(5*7)+(4*4)+(3*1)+(2*1)+(1*6)=146
146 % 10 = 6
So 67741-16-6 is a valid CAS Registry Number.

67741-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(cyanomethyl)phenyl acetate

1.2 Other means of identification

Product number -
Other names 4-acetoxyphenylacetonitrile

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:67741-16-6 SDS

67741-16-6Relevant articles and documents

Selective Dual-Channel Imaging on Cyanostyryl-Modified Azulene Systems with Unimolecularly Tunable Visible–Near Infrared Luminescence

Zhou, Yunyun,Zhuang, Yaping,Li, Xin,?gren, Hans,Yu, Lin,Ding, Jiandong,Zhu, Liangliang

, p. 7642 - 7647 (2017)

Although organic light-emitting molecules have received a growing attention and applicability in modern bioimaging science, the design and control of complex photoluminescent properties in unimolecularly selective imaging remains a challenging topic. Cons

A sensitive AIEE probe for amphiphilic compounds

Palakollu, Veerabhadraiah,Vasu, Anuji K.,Thiruvenkatam, Vijay,Kanvah, Sriram

, p. 4588 - 4594 (2016/06/09)

α-Cyanostilbene substituted with dimethylaniline and hydroxyl groups exhibits profound intensity enhanced bathochromic shifts in an aqueous medium as compared to organic solvents. These conspicuous emission changes are attributed to aggregation as a conse

Cholesterol-tethered AIEE fluorogens: Formation of self-assembled nanostructures

Palakollu, Veerabhadraiah,Kanvah, Sriram

, p. 33049 - 33057 (2015/04/27)

Design and synthesis of cholesterol conjugated chromophores exhibiting intramolecular charge transfer (ICT) and Aggregation Induced Enhanced Emission (AIEE) is described. Cholesterol conjugated α-cyanostilbene exhibits weak emission in organic solvents bu

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