Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2497-91-8

Post Buying Request

2497-91-8 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2497-91-8 Usage

Chemical Properties

light beige granular powder

Check Digit Verification of cas no

The CAS Registry Mumber 2497-91-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,9 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2497-91:
(6*2)+(5*4)+(4*9)+(3*7)+(2*9)+(1*1)=108
108 % 10 = 8
So 2497-91-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H3ClN2O6/c8-6-4(7(11)12)1-3(9(13)14)2-5(6)10(15)16/h1-2H,(H,11,12)/p-1

2497-91-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A15675)  2-Chloro-3,5-dinitrobenzoic acid, 97% (dry wt.), may cont. up to ca 5% water   

  • 2497-91-8

  • 25g

  • 230.0CNY

  • Detail
  • Alfa Aesar

  • (A15675)  2-Chloro-3,5-dinitrobenzoic acid, 97% (dry wt.), may cont. up to ca 5% water   

  • 2497-91-8

  • 100g

  • 671.0CNY

  • Detail
  • Alfa Aesar

  • (A15675)  2-Chloro-3,5-dinitrobenzoic acid, 97% (dry wt.), may cont. up to ca 5% water   

  • 2497-91-8

  • 500g

  • 1785.0CNY

  • Detail

2497-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-3,5-dinitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 3,5-dinitro-2-chlorobenzoic acid

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:2497-91-8 SDS

2497-91-8Relevant articles and documents

Benzoxazinone derivatives and their use as antibacterial agents

-

Paragraph 0117-0120, (2018/09/12)

The invention discloses benzoxazinone derivatives, a synthesis method and applications thereof. The derivatives can be used as an antibacterial agent for treating infectious diseases caused by bacteria, especially tuberculosis (TB) caused by mycobacterium. Specifically, the invention relates to compounds represented by the formula (I), pharmaceutically acceptable salts thereof, and a pharmaceutical composition comprising the provided compounds; wherein the R1 to R4 are defined in the description. The invention aim to prepare novel compounds capable of inhibiting the mycobacterium activity, the compounds can be used as a potential novel drug for treating infectious diseases caused by bacteria, moreover, the compounds can be used to treat or prevent tuberculosis (TB) caused by mycobacterium, at the same time the problems related with drug resistance can be solved, and the drug metabolism property can be improved on the basis that the mycobacterium tuberculosis resistant activity is not influenced.

Anti-viral and anti-cancer agents

-

, (2008/06/13)

2-chloro-5-nitrobenzoic acid and various other chloro and nitro substitute benzoic acid derivatives are disclosed for administration in tablet or injectable solution form for the prophylaxis and therapy of neoplasm or viral infection. The active compounds have surprising efficacy in various treatment regimes and have particular application to HIV-infection and demonstrate various beneficial effects, including regression of lesions in HIV-related Kaposi's sarcoma.

Synthesis of Polynitrodiazophenols

Atkins, Ronald L.,Wilson, William S.

, p. 2572 - 2578 (2007/10/02)

The formation of diazophenols by nitration of suitably substituted anilines and rearrangement of the nitroaromatic nitramines so formed is presented.The scope of the reaction is discussed, and a mechanism for the nitramine/diazophenol rearrangement is proposed which is consistent with 15N-labeling experiments.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 2497-91-8