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68109-89-7

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68109-89-7 Usage

General Description

3-[(E)-2-(Dimethylamino)ethenyl]-2-nitrobenzoic acid methyl ester, also known as DCM, is a chemical compound commonly used as a marker for apoptosis in biological research. It is a fluorescent dye that binds to DNA and can be used for staining cells in flow cytometry assays. DCM has a wide range of applications in biomedical and pharmaceutical research, including studying the progression of cancer and other diseases. Additionally, it is used as a tracer in environmental research to study the fate and transport of chemicals in natural systems. Overall, DCM is a versatile compound that plays an important role in the fields of biology, medicine, and environmental science.

Check Digit Verification of cas no

The CAS Registry Mumber 68109-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,0 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68109-89:
(7*6)+(6*8)+(5*1)+(4*0)+(3*9)+(2*8)+(1*9)=147
147 % 10 = 7
So 68109-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O4/c1-13(2)8-7-9-5-4-6-10(12(15)18-3)11(9)14(16)17/h4-8H,1-3H3/b8-7+

68109-89-7SDS

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 methyl 3-[(E)-2-(dimethylamino)ethenyl]-2-nitrobenzoate

1.2 Other means of identification

Product number -
Other names CCG-7415

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:68109-89-7 SDS

68109-89-7Relevant articles and documents

A prepares Nepal to pull handkerchief Nepal method (by machine translation)

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Paragraph 0053; 0054, (2017/07/23)

The invention discloses a compound 2 - [4 - ((3S) - 3 - piperidinyl) phenyl] - 2H - indazole - 7 - carboxamide preparation method, through the 4 - nitro phenylpyridyl with reaction produced animal pen halogenphenmethyl season ammonium salt, by sodium borohydride reduction of the pyridine quaternary ammonium salt, in the palladium reagent obtained under the action of the 3 - (4 - aminophenyl) piperidine, in the chiral reagent obtained under the action of the (S)- 3 - (4 - halophenyl) piperidine, with 3 - formyl - 2 - nitro-benzoic acid methyl ester condensation and in sodium azide formed under the action of powder medicine, after preparing the amine Niraparib (molecular entity is: 2 - [4 - ((3S) - 3 - piperidinyl) phenyl] - 2H - indazole - 7 - carboxamide). (by machine translation)

Development of a fit-for-purpose large-scale synthesis of an oral PARP inhibitor

Wallace, Debra J.,Baxter, Carl A.,Brands, Karel J. M.,Bremeyer, Nadine,Brewer, Sarah E.,Desmond, Richard,Emerson, Khateeta M.,Foley, Jennifer,Fernandez, Paul,Hu, Weifeng,Keen, Stephen P.,Mullens, Peter,Muzzio, Daniel,Sajonz, Peter,Tan, Lushi,Wilson, Robert D.,Zhou, George,Zhou, Guoyue

experimental part, p. 831 - 840 (2012/07/03)

Compound (1) a poly(ADP-ribose)polymerase (PARP) inhibitor has been made by a fit-for-purpose large-scale synthesis using either a classical resolution or chiral chromatographic separation. The development and relative merits of each route are discussed,

Thromboxane A2 synthetase inhibitors with histamine H1-blocking activity: Synthesis and evaluation of a new series of indole derivatives

Kamiya,Matsui,Shirahase,Nakamura,Wada,Kanda,Shimaji,Kakeya

, p. 1692 - 1695 (2007/10/03)

A novel series of N-substituted 3-(1H-imidazol-1-ylmethyl)indole carboxylic acid derivatives were prepared and evaluated for thromboxane A2 (TXA2) synthetase-inhibitory and histaminergic H1-blocking activity. Among the compounds synthesized, indole-6-carboxylic acid derivatives showed higher activities than the other positional isomers of carboxylic acid. 1-[3-(4- Benzhydryl-1-piperazinyl)propyl]-3-(1H-imidazol-1-ylmethyl)-1H-indole-6- carboxylic acid (12) had the strongest thromboxane synthetase inhibitory activity (IC50 = 5 x 10-8 M) and H1-blocking activity (IC50 = 8 x 10- 9 M).

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