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16726-67-3

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16726-67-3 Usage

Chemical Properties

white solid

Check Digit Verification of cas no

The CAS Registry Mumber 16726-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,2 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16726-67:
(7*1)+(6*6)+(5*7)+(4*2)+(3*6)+(2*6)+(1*7)=123
123 % 10 = 3
So 16726-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H7BrO2/c12-10-6-2-3-7-8(10)4-1-5-9(7)11(13)14/h1-6H,(H,13,14)

16726-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromonaphthalene-1-Carboxylic Acid

1.2 Other means of identification

Product number -
Other names 1-Naphthalenecarboxylic acid, 5-bromo-

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:16726-67-3 SDS

16726-67-3Relevant articles and documents

A microporous lanthanide-tricarboxylate framework with the potential for purification of natural gas

He, Yabing,Xiong, Shunshun,Chen, Banglin,Xiang, Shengchang,Zhang, Zhangjing,Fronczek, Frank R.,Krishna, Rajamani,O'Keeffe, Michael

, p. 10856 - 10858,3 (2012)

A novel robust three-dimensional lanthanide organic framework with high thermal stability has been demonstrated to exhibit the potential for purification of natural gas in nearly pure form from an 8-component gas mixture at room temperature.

Oxime ether derivative and preparation method and application thereof

-

Paragraph 0068; 0069; 0075; 0077; 0084; 0085; 0092; 0093, (2018/08/03)

The invention discloses oxime ether derivative and a preparation method and application thereof. The oxime ether derivative is shown as any one of 1) to 6), wherein the 1) is 5-bromine-1-naphthalene formaldehyde oxime ether, the 2) is 5-methoxy-1-naphthalene formaldehyde oxime ether, the 3) is 5-phenyl-1-naphthalene formaldehyde oxime ether, the 4) is 5-p-methoxyphenyl-1-naphthalene formaldehyde oxime ether, the 5) is 5-p-ethoxyphenyl-1-naphthalene formaldehyde oxime ether, and the 6) is 3-5-ethyl(E)-1-naphthalene formaldehyde oxime ether. According to the oxime ether derivative, 1-naphthoic acid is utilized as a raw material; the oxime ether derivative is synthesized by coupling reaction of Suzuki reaction, Heck reaction and the like, acylation reaction and oximation reaction. The compound disclosed by the invention has good antineoplastic activity and has a very good prospect in medicinal development.

Synthesis of monofluorinated 1-(naphthalen-1-yl)piperazines

Repine, Joseph T.,Johnson, Douglas S.,White, Andrew D.,Favor, David A.,Stier, Michael A.,Yip, Judy,Rankin, Trent,Ding, Qizhu,Maiti, Samarendra N.

, p. 5539 - 5541 (2008/02/13)

A series of regioisomerically monofluorinated 1-(naphthalen-1-yl)piperazines is described.

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