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O-(4-Formylphenyl)carbamothioicaciddimethylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84265-06-5

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84265-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84265-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,6 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84265-06:
(7*8)+(6*4)+(5*2)+(4*6)+(3*5)+(2*0)+(1*6)=135
135 % 10 = 5
So 84265-06-5 is a valid CAS Registry Number.

84265-06-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Carbamothioic acid, dimethyl-, O-(4-formylphenyl) ester

1.2 Other means of identification

Product number -
Other names O-(4-FORMYLPHENYL) DIMETHYLTHIOCARBAMATE

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:84265-06-5 SDS

84265-06-5Downstream Products

84265-06-5Relevant academic research and scientific papers

Rational design of an HClO-specific triggered self-immolative fluorescent turn-on sensor and its bioimaging applications

Li, Hui-Jing,Liu, Quanze,Lu, Xuhao,Wang, Xiao-Bo,Wu, Yan-Chao,Zhang, Da-Long

, p. 8793 - 8800 (2021/11/16)

The development of a rapid and intuitive method for the detection of a specific small molecule biomarker is important for understanding the pathogenesis of relevant diseases. Described here is the design and evaluation of an HClO-specific triggered self-immolative fluorescent sensor (RESClO) based on the structure of an N-protected Resorufin dye. Due to the interrupted π-conjugated structure of the Resorufin dye, the free sensor showed very weak absorption and fluorescence. It can quickly complete the response to HClO (within 10 s) with high selectivity and sensitivity (LOD = 16.8 nM) in aqueous solution. The sensor can be made into test strips to quickly detect HClO in the environment by obvious changes in color and fluorescence. It was successfully used for bioimaging of exogenous and endogenous HClO in cells and zebra fish. More importantly, it can also be used for visual imaging of mouse arthritis models. Thus, sensor RESClO can provide a simple and promising visual analytical tool for the detection of HClO in the environment and the early diagnosis of HClO-mediated related diseases. This journal is

Near-infrared xanthene fluorescent probe as well as preparation method and application thereof

-

Paragraph 0056-0057, (2021/08/28)

The invention provides a near-infrared xanthene fluorescent probe as well as a preparation method and application thereof, and belongs to the technical field of biological small molecule detection. The near-infrared xanthene fluorescent probe (a compound

COMPOUNDS FOR THE PREVENTION AND TREATMENT OF MEDICAL DISORDERS AND USES THEREOF

-

Paragraph 0183; 0184, (2019/02/15)

Aspects of the invention relate to compounds, pharmaceutical compositions, methods for the manufacturing of compounds and methods for treatment of various disorders mediated at least in part by one or more galectins.

A Mechanism-Based Approach to Screening Metagenomic Libraries for Discovery of Unconventional Glycosidases

Nasseri, Seyed Amirhossein,Betschart, Leo,Opaleva, Daria,Rahfeld, Peter,Withers, Stephen G.

supporting information, p. 11359 - 11364 (2018/08/28)

Functional metagenomics has opened new opportunities for enzyme discovery. To exploit the full potential of this new tool, the design of selective screens is essential, especially when searching for rare enzymes. To identify novel glycosidases that employ cleavage strategies other than the conventional Koshland mechanisms, a suitable screen was needed. Focusing on the unsaturated glucuronidases (UGLs), it was found that use of simple aryl glycoside substrates did not allow sufficient discrimination against β-glucuronidases, which are widespread in bacteria. While conventional glycosidases cannot generally hydrolyze thioglycosides efficiently, UGLs follow a distinct mechanism that allows them to do so. Thus, fluorogenic thioglycoside substrates featuring thiol-based self-immolative linkers were synthesized and assessed as selective substrates. The generality of the approach was validated with another family of unconventional glycosidases, the GH4 enzymes. Finally, the utility of these substrates was tested by screening a small metagenomic library.

Porphyrin compound and preparation method and application thereof in surface enhanced Raman probe

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Paragraph 0034; 0035; 0037, (2017/01/17)

The invention relates to a porphyrin compound and a preparation method and an application thereof in a surface enhanced Raman probe. The porphyrin compound is 5-[4-(N,N-dimethylamino formyl)phenyl]-15-(4-carboxyl phenyl)porphyrin, and has the structure represented by the formula (I). One end of the prepared porphyrin compound is a carboxyl group which can be firmly adsorbed on the surface of titanium dioxide, and the other end of the prepared porphyrin compound is thiol ester which is adsorbed on a silver surface to form an S-Ag bond. Titanium dioxide nanoparticles and silver nanoparticles form a stable and ordered composite material under connective action of the molecule, and a stable and ordered SERS substrate is formed. The mark molecule is not only a template agent for the substrate but also has a stable signal on the substrate, and has a broad application prospect.

A thiol-thiosulfonate reaction providing a novel strategy for turn-on thiol sensing

Ge, Chunpo,Wang, Hao,Zhang, Baoxin,Yao, Juan,Li, Xinming,Feng, Weimin,Zhou, Panpan,Wang, Yawen,Fang, Jianguo

supporting information, p. 14913 - 14916 (2015/10/06)

The first thiol-specific turn-on probe, BODIPY-TS, utilizing a thiosulfonate scaffold as the thiol recognition unit was reported. BODIPY-TS displays low toxicity, and features high sensitivity, fast response and quantitative reaction towards thiols. The structural novelty of BODIPY-TS would guide the development of novel thiol probes.

ISOXAZOLE DERIVATIVE HAVING AGONISTIC ACTIVITY AGAINST PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR

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Page/Page column 106, (2010/11/23)

A compound of formula (I) : (wherein R1-R10 are each independently hydrogen, halogen, optionally substituted lower alkyl or the like, X1 is -O-, -S-, -NR11- (wherein R11 is hydrogen, lower alkyl or the like), -CR12R13CO-, -(CR12R13)mO-, -O(CR12R13)m- (wherein R12 and R13 are each independently hydrogen or lower alkyl and m is a integer between 1 and 3) or the like, X2 is a bond, -O-, -S-, -NR14- (wherein R14 is hydrogen, lower alkyl or the like, R14 and R6 can be taken together with the neighboring atom to form a ring) or -CR15R16-(wherein R15 and R16 are each independently hydrogen or lower alkyl, R15 and R6 or R10 can be taken together with the neighboring carbon atom to form a ring, R16 and R9 can be joined together to form a bond), X3 is COOR17, C( = NR17)NR18OR19 or the like), a pharmaceutically acceptable salt or a solvate thereof.

Tetrahydronaphthalene and indane compounds useful as anti-tumor agents

-

, (2008/06/13)

This invention is directed to tetrahydronaphthalene and indane compounds and processes thereto. These compounds are useful as tumor inhibiting agents, in the treatment of neoplasms and dermatological conditions.

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