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Benzenesulfonamide, N-3-butenyl-2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90870-33-0

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90870-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90870-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,7 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90870-33:
(7*9)+(6*0)+(5*8)+(4*7)+(3*0)+(2*3)+(1*3)=140
140 % 10 = 0
So 90870-33-0 is a valid CAS Registry Number.

90870-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-but-3-enyl-2-nitrobenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-(but-3-enyl)-2-nitrobenzenesulfonamide

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:90870-33-0 SDS

90870-33-0Downstream Products

90870-33-0Relevant academic research and scientific papers

Two-step activity-based protein profiling of diacylglycerol lipase

Van Rooden, Eva J.,Kreekel, Roy,Hansen, Thomas,Janssen, Antonius P. A.,Van Esbroeck, Annelot C. M.,Den Dulk, Hans,Van Den Berg, Richard J. B. H. N.,Codée, Jeroen D. C.,Van Der Stelt, Mario

supporting information, p. 5250 - 5253 (2018/08/03)

Diacylglycerol lipases (DAGL) produce the endocannabinoid 2-arachidonoylglycerol, a key modulator of neurotransmitter release. Chemical tools that visualize endogenous DAGL activity are desired. Here, we report the design, synthesis and application of a triazole urea probe for DAGL equipped with a norbornene as a biorthogonal handle. The activity and selectivity of the probe was assessed with activity-based protein profiling. This probe was potent against endogenous DAGLα (IC50 = 5 nM) and it was successfully applied as a two-step activity-based probe for labeling of DAGLα using an inverse electron-demand Diels-Alder ligation in living cells.

SELECTIVELY SUBSTITUTED QUINOLINE COMPOUNDS

-

Paragraph 0180; 0702, (2015/04/21)

Embodiments of the disclosure relate to selectively substituted quinoline compounds that act as antagonists or inhibitors for Toll-like receptors 7 and/or 8, and their use in pharmaceutical compositions effective for treatment of systemic lupus erythematosus (SLE) and lupus nephritis.

Synthesis of natural-product-like molecules with over eighty distinct scaffolds

Morton, Daniel,Leach, Stuart,Cordier, Christopher,Warriner, Stuart,Nelson, Adam

supporting information; experimental part, p. 104 - 109 (2009/04/12)

(Chemical Equation Presented) Seeking scaffold diversity: A synthetic approach for the combinatorial variation of the scaffolds of small molecules is described. Using just six basic reaction types, compounds with 84 distinct scaffolds were prepared. The c

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