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2H-1,4-Benzoxazine, 6-nitro-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112182-36-2

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112182-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112182-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,8 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112182-36:
(8*1)+(7*1)+(6*2)+(5*1)+(4*8)+(3*2)+(2*3)+(1*6)=82
82 % 10 = 2
So 112182-36-2 is a valid CAS Registry Number.

112182-36-2Downstream Products

112182-36-2Relevant academic research and scientific papers

Design, synthesis, and biological activity of novel Magmas inhibitors

Jubinsky, Paul T.,Short, Mary K.,Ghanem, Mohmoud,Das, Bhaskar C.

, p. 3479 - 3482 (2011)

Magmas (mitochondria associated, granulocyte-macrophage colony stimulating factor signaling molecule), is a highly conserved and essential gene, expressed in all cell types. We designed and synthesized several small molecule Magmas inhibitors (SMMI) and a

RETINOIC ACID RECEPTOR ANTAGONISTS AS CHAPERONE-MEDIATED AUTOPHAGY MODULATORS AND USES THEREOF

-

Paragraph 0081; 0082; 0122, (2015/06/24)

Compounds, compositions and methods are provided for selectively activating chaperone-mediated autophagy (CMA), protecting cells from oxidative stress, proteotoxicity and lipotoxicity, and/or antagonizing activity of retinoic acid receptor alpha (RARα) in

Direct organocatalytic asymmetric mannich addition of 3-substituted-2H-1,4- benzoxazines: Access to tetrasubstituted carbon stereocenters

Wang, You-Qing,Zhang, Yongna,Pan, Kun,You, Junxiong,Zhao, Jin

supporting information, p. 3381 - 3386 (2013/12/04)

3-Substituted-2H-1,4-benzoxazines undergo a highly enantioselective direct Mannich reaction with acetone in the presence of an L-proline catalyst at room temperature. The corresponding N-heterocycles with α-tetrasubstituted carbon stereocenters were obtai

Design, synthesis and biological evaluation of 2H-benzo[b][1,4] oxazine derivatives as hypoxia targeted compounds for cancer therapeutics

Das, Bhaskar C.,Madhukumar, Ankanahlli V.,Anguiano, Jaime,Mani, Sridhar

supporting information; experimental part, p. 4204 - 4206 (2010/04/05)

A small library of 2H-benzo[b][1,4] oxazine derivative was synthesized and their biological activity was tested on HepG2 cells under normoxic and hypoxic conditions. From preliminary screening, we found compound 10 and 11 specifically inhibit hypoxic canc

Synthesis and Anthelmintic Activity of some New Isothiocyanates, Carbamates and N'-Furoylthioureas derived from 6-Amino-3-aryl/heteroaryl-2H-1,4-benzoxazines

Shridhar, D. R.,Rao, K. Srinivasa,Rastogi, K.,Gnadhi, S. S.

, p. 761 - 763 (2007/10/02)

Several new isothiocyanates (3a-k), carbamates (4a-k) and N'-furoylthioureas (5a-k) derived from 6-amino-3-aryl/heteroaryl-2H-1,4-benzoxazines have been synthesised and screened for their anthelmintic activity.

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