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Benzamide, 2-chloro-N-methyl-5-nitro-, also known as 2-Chloro-N-methyl-5-nitrobenzamide, is an organic compound with the chemical formula C8H8ClN3O2. It is a derivative of benzamide, featuring a chlorine atom at the 2nd position, a nitro group at the 5th position, and a methyl group attached to the nitrogen atom. Benzamide, 2-chloro-N-methyl-5-nitro- is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used in chemical research and as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its potential applications and reactivity, it is important to handle Benzamide, 2-chloro-N-methyl-5-nitro- with care, adhering to proper safety protocols.

85469-93-8

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85469-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85469-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,6 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85469-93:
(7*8)+(6*5)+(5*4)+(4*6)+(3*9)+(2*9)+(1*3)=178
178 % 10 = 8
So 85469-93-8 is a valid CAS Registry Number.

85469-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-methyl-5-nitrobenzamide

1.2 Other means of identification

Product number -
Other names N1-methyl-2-chloro-5-nitrobenzamide

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:85469-93-8 SDS

85469-93-8Relevant academic research and scientific papers

Covalent Occlusion of the RORγt Ligand Binding Pocket Allows Unambiguous Targeting of an Allosteric Site

Meijer, Femke A.,Van Den Oetelaar, Maxime C. M.,Doveston, Richard G.,Sampers, Ella N. R.,Brunsveld, Luc

supporting information, p. 631 - 639 (2021/04/07)

The nuclear receptor RORγt is a key positive regulator in the differentiation and proliferation of T helper 17 (Th17) cells and the production of proinflammatory cytokines like IL-17a. Dysregulation of this pathway can result in the development of various

GDC-0449-A potent inhibitor of the hedgehog pathway

Robarge, Kirk D.,Brunton, Shirley A.,Castanedo, Georgette M.,Cui, Yong,Dina, Michael S.,Goldsmith, Richard,Gould, Stephen E.,Guichert, Oivin,Gunzner, Janet L.,Halladay, Jason,Jia, Wei,Khojasteh, Cyrus,Koehler, Michael F.T.,Kotkow, Karen,La, Hank,LaLonde, Rebecca L.,Lau, Kevin,Lee, Leslie,Marshall, Derek,Marsters Jr., James C.,Murray, Lesley J.,Qian, Changgeng,Rubin, Lee L.,Salphati, Laurent,Stanley, Mark S.,Stibbard, John H.A.,Sutherlin, Daniel P.,Ubhayaker, Savita,Wang, Shumei,Wong, Susan,Xie, Minli

scheme or table, p. 5576 - 5581 (2010/04/05)

SAR for a wide variety of heterocyclic replacements for a benzimidazole led to the discovery of functionalized 2-pyridyl amides as novel inhibitors of the hedgehog pathway. The 2-pyridyl amides were optimized for potency, PK, and drug-like properties by modifications to the amide portion of the molecule resulting in 31 (GDC-0449). Amide 31 produced complete tumor regression at doses as low as 12.5 mg/kg BID in a medulloblastoma allograft mouse model that is wholly dependent on the Hh pathway for growth and is currently in human clinical trials, where it is initially being evaluated for the treatment of BCC.

Aryl triazines as LPAAT-SS inhibitors and uses thereof

-

, (2008/06/13)

The invention relates to aryl triazines and uses thereof, including to inhibit lysophosphatidic acid acyltransferase β (LPAAT-β) activity and/or proliferation of cells such as tumor cells.

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