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84998-84-5

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84998-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84998-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,9 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84998-84:
(7*8)+(6*4)+(5*9)+(4*9)+(3*8)+(2*8)+(1*4)=205
205 % 10 = 5
So 84998-84-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Br3O3/c9-4-1-5(10)8(6(11)2-4)14-3-7(12)13/h1-2H,3H2,(H,12,13)

84998-84-5SDS

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-(2,4,6-tribromophenoxy)acetic acid

1.2 Other means of identification

Product number -
Other names 2.4.6-Tribrom-phenylaetherglykolsaeure

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:84998-84-5 SDS

84998-84-5Relevant articles and documents

Synthesis and biological evaluation of some novel 2-mercaptobenzothiazoles carrying 1,3,4-oxadiazole, 1,3,4-thiadiazole and 1,2,4-triazole moieties

Azam, M. Afzal,Suresh, Bhojraj,Kalsi, Sandip S.,Antony, A. Shinesh

scheme or table, p. 114 - 122 (2011/06/09)

Several 2-mercaptobenzothiazole derivatives containing 1,3,4-oxadiazoles, 1,2,4-triazoles and 1,3,4-thiadiazoles at the second position were synthesized. Some of these synthesized compounds were evaluated for their in vivo analgesic, anti-inflammatory, acute toxicity and ulcerogenic actions. Some of the tested compounds showed significant analgesic and anti-inflammatory activities. Two of the compounds showed significant gastrointestinal protection compared to the standard drug diclofenac sodium. The compounds were also tested for their in vitro antimicrobial activity with most displaying selective activity against the Gram-negative bacteria Pseudomonas aeruginosa. In the present investigation the tested compounds did not possess antifungal activity.

Synthesis and Antimicrobial Activity of N-piperazines/morpholines

Chaurasia, Sunita,Srivastava, Savitri D.

, p. 45 - 46 (2007/10/02)

-

Synthesis of some new bio-active aryl amides

Srivastava,Purohit,Srivastava,Jain,Khubchandani

, p. 358 - 359 (2007/10/02)

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