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63697-96-1

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63697-96-1 Usage

Uses

4-?Ethynylbenzaldehyde is commonly used in solar cells as the acceptor unit.

Synthesis Reference(s)

The Journal of Organic Chemistry, 46, p. 2280, 1981 DOI: 10.1021/jo00324a015

Check Digit Verification of cas no

The CAS Registry Mumber 63697-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,9 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63697-96:
(7*6)+(6*3)+(5*6)+(4*9)+(3*7)+(2*9)+(1*6)=171
171 % 10 = 1
So 63697-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H6O/c1-2-8-3-5-9(7-10)6-4-8/h1,3-7H

63697-96-1 Well-known Company Product Price

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  • TCI America

  • (E0987)  4-Ethynylbenzaldehyde  >98.0%(GC)

  • 63697-96-1

  • 1g

  • 1,390.00CNY

  • Detail

63697-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Ethynylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-ETHYNYLBENZALDEHYDE

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:63697-96-1 SDS

63697-96-1Relevant articles and documents

A fluorescent probe for the 3′-overhang of telomeric DNA based on competition between two interstrand G-quadruplexes

Kim, Ki Tae,Kim, Byeang Hyean

, p. 1717 - 1719 (2013)

A 6-mer oligonucleotide containing a fluorescent BodU moiety has been used as a novel fluorescent probe for the 3′-overhang of telomeric DNA based on competition between non-fluorescent tetramolecular and fluorescent (3+1) intermolecular G-quad

Synthesis, characterization, electrochemistry and photophysical studies of rhenium(I) tricarbonyl diimine complexes with carboxaldehyde alkynyl ligands Dedicated to Professor Claude Lapinte for his contribution to organometallic chemistry.

Lam, Siu-Tung,Zhu, Nianyong,Au, Vonika Ka-Man,Yam, Vivian Wing-Wah

, p. 10 - 16 (2015)

A class of rhenium(I) tricarbonyl diimine complexes with carboxaldehyde alkynyl ligands, [Re(CO)3(N^N)(CC-C6H4-CHO)] (N^N = α,α′-diimine ligand), has been successfully synthesized and characterized, and the X-ray crystal structure of one of the complexes has been determined. Electrochemical and photophysical studies have been performed to study the effect of the variation of the diimine ligand on the redox and optical properties of the rhenium(I) complexes.

Ionic liquids enhanced alkynyl schiff bases derivatives of fipronil synthesis and their cytotoxicity studies

Liu, Xiu,Huang, Linya,Chen, Hongjun,Li, Na,Yan, Chao,Jin, Chenzhong,Xu, Hanhong

, (2019)

To obtain highly selective toxic derivatives of fipronil, a series of Schiff bases with an alkynyl group (3a–3k) were designed and synthesized from 4-ethynylbenzaldehyde (2) and 4-substituted 5-amino-N-arylpyrazole (1a–1k) via a nucleophilic addition elim

Helical poly(phenylacetylene)s containing schiff-base and amino groups: Synthesis, secondary structures, and responsiveness to benzoic acid

Zhang, Yu,Gao, Keke,Zhao, Zhongfu,Yue, Dongmei,Hu, Yanming,Masuda, Toshio

, p. 5248 - 5256 (2013)

Novel acetylenic monomers containing Schiff-base and amino groups, (S)-N-(4-ethynylbenzylidene)-1-phenylethanamine (1a), (R)-N-(4- ethynylbenzylidene)-1-phenylethanamine (1b), N-(4-ethynylbenzylidene)-1- phenylethanamine (1c), (R)-N-(4-ethynylbenzyl)-1-ph

Combining photo-redox and enzyme catalysis for the synthesis of 4H-pyrimido[2,1-b] benzothiazole derivatives in one pot

Yu, Yuan,Lu, Wei-Fan,Yang, Zeng-Jie,Wang, Na,Yu, Xiao-Qi

supporting information, (2020/12/25)

A novel strategy combining visible-light and enzyme catalysis in one pot for the synthesis of 4H-pyrimido[2,1-b] benzothiazole derivatives from alcohols is described for the first time. Fourteen 4H-pyrimido[2,1-b] benzothiazole derivatives were prepared with yields of up to 98% under mild reaction conditions by a simple operation. The photoorgano catalyst rose Bengal (rB) was employed to oxyfunctionalise alcohols to aldehydes. Compared with aldehydes, alcohols with more stable properties and lower cost, thus we used photocatalysis to oxidize alcohols into aldehydes. Next, the enzyme was used to further catalyze the reaction of Biginelli to produce the target product of 4H-pyrimidine [2,1-b] benzothiazole. Experimental results show that this method provides a more efficient and eco-friendly strategy for the synthesis of 4H-pyrimido[2,1-b] benzothiazole derivatives.

RET INHIBITORS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF

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Paragraph 00324-00325, (2020/07/06)

Provided herein are a RET inhibitor, a pharmaceutical composition thereof and uses thereof. In particular, provided is a compound having Formula (I) or a stereoisomer, a geometric isomer, a tautomer, an N-oxide, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof. Provided is a pharmaceutical composition comprising the compound, and uses of the compound and pharmaceutical composition thereof for the preparation of a medicament, in particular for treatment and prevention of RET-related diseases and conditions, including cancer, irritable bowel syndrome, and/or pain associated with irritable bowel syndrome.

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