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4-(tert-Butyldimethylsilyl)oxy-2-nitroaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

215656-99-8

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215656-99-8 Usage

Chemical Properties

Brown Solid

Uses

Intermediate in the production of antithrombotic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 215656-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,6,5 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 215656-99:
(8*2)+(7*1)+(6*5)+(5*6)+(4*5)+(3*6)+(2*9)+(1*9)=148
148 % 10 = 8
So 215656-99-8 is a valid CAS Registry Number.

215656-99-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[tert-butyl(dimethyl)silyl]oxy-2-nitroaniline

1.2 Other means of identification

Product number -
Other names -

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:215656-99-8 SDS

215656-99-8Relevant academic research and scientific papers

Synthesis and bioluminescence of electronically modified and rotationally restricted colour-shifting infraluciferin analogues

Anderson, James C.,Chang, Chia-Hao,Jathoul, Amit P.,Syed, Aisha J.

, p. 347 - 356 (2019/01/04)

Synthetic nIR emitting luciferins can enable clearer bioluminescent imaging in blood and tissue. A limiting factor for all synthetic luciferins is their reduced light output with respect to D-luciferin. In this work we explore a design feature of whether

FUSED TRICYCLIC COMPOUNDS AS RAF KINASE INHIBITORS

-

Paragraph 0209; 0294-0295-0296, (2021/02/16)

Provided are certain fused tricyclic compounds and salts thereof, compositions thereof, and methods of use therefor.

Condensed tricyclic compounds as RAF kinase inhibitors

-

Paragraph 0358; 0495; 0496; 0497; 0498; 0499, (2016/10/07)

The invention provides certain condensed tricyclic compounds as well as salt, compositions and application methods thereof.

CONDENSED TRICYCLIC COMPOUNDS AS Raf KINASE INHIBITORS

-

Paragraph 0187; 0188, (2017/01/05)

PROBLEM TO BE SOLVED: To provide specific tricyclic compounds that can be useful for inhibiting Raf kinase and for treating disorders mediated by Raf kinase. SOLUTION: A compound is represented by the general formula 1 in the figure. (Q is C or N; W is C or N; X is CH2 or O; Y is NR12, O or S; Z is O, S, NR13, CO, SO, SO2 or CR13R14; R1 to R6 are each independently hydrogen, halogen, haloalkyl, alkyl or the like.) SELECTED DRAWING: None COPYRIGHT: (C)2017,JPO&INPIT

Membrane-permeable Mn(III) complexes for molecular magnetic resonance imaging of intracellular targets

Barandov, Ali,Bartelle, Benjamin B.,Gonzalez, Beatriz A.,White, William L.,Lippard, Stephen J.,Jasanoff, Alan

supporting information, p. 5483 - 5486 (2016/06/01)

Intracellular compartments make up roughly two-thirds of the body, but delivery of molecular imaging probes to these spaces can be challenging. This situation is particularly true for probes designed for detection by magnetic resonance imaging (MRI), a hi

FUSED TRICYCLIC COMPOUNDS AS RAF KINASE INHIBITORS

-

Paragraph 0331-0333, (2015/02/25)

Provided are certain fused tricyclic compounds and salts thereof, compositions thereof, and methods of use therefor.

RADIOACTIVE FLUORINE-LABELED QUINOXALINE COMPOUND

-

Paragraph 0052-0053, (2014/04/03)

Provided is a compound effective as a diagnostic imaging probe targeting amyloid and an agent for Alzheimer's disease diagnosis including the compound.

[5,6]HETEROCYCLIC COMPOUND

-

Paragraph 0083-0084, (2013/03/26)

Abstract: An object of the present invention is to provide a novel low molecular weight compound exhibiting an osteogenesis-promoting action. This object is achieved by a compound having the general formula (I) or a pharmacologically acceptable salt thereof. In the general formula (I), R1 and R2 represent hydrogen atoms, and the like; R3 represents a hydrogen atom, and the like; X, Y, and Z represent nitrogen atoms, and the like; A represents a phenylene group, and the like; n represents 1 or 2, and the like; and V and W represent oxygen atoms, and the like.

FUSED TRICYCLIC COMPOUNDS AS RAF KINASE INHIBITORS

-

Page/Page column 61, (2013/07/19)

Provided are certain fused tricyclic compounds and salts thereof, compositions thereof, and methods of use therefor.

Structure-activity relationships and in vivo evaluation of quinoxaline derivatives for PET imaging of β-amyloid plaques

Yoshimura, Masashi,Ono, Masahiro,Matsumura, Kenji,Watanabe, Hiroyuki,Kimura, Hiroyuki,Cui, Mengchao,Nakamoto, Yuji,Togashi, Kaori,Okamoto, Yoko,Ihara, Masafumi,Takahashi, Ryosuke,Saji, Hideo

supporting information, p. 596 - 600 (2013/07/26)

This letter describes the synthesis, structure-activity relationships, and in vivo evaluation of a new series of 2-phenylquinoxaline (PQ) derivatives for imaging β-amyloid (Aβ) plaques in Alzheimer's disease (AD). In experiments in vitro, the affinity of

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