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176690-44-1

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176690-44-1 Usage

General Description

2-Pyridin-3-yl-benzaldehyde is a chemical compound with the molecular formula C12H9NO. It is a yellowish solid with a characteristic aromatic odor, and it is commonly used as a building block in the synthesis of various organic compounds. 2-Pyridin-3-yl-benzaldehyde is often utilized in the production of pharmaceuticals, agrochemicals, and dyes. It is known for its ability to participate in a variety of chemical reactions, including alkylation, acylation, and condensation reactions. The compound is also used as a reagent for the extraction and determination of metal ions in various analytical procedures. Overall, 2-Pyridin-3-yl-benzaldehyde has a wide range of applications in the chemical industry and is an important intermediate in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 176690-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,6,9 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 176690-44:
(8*1)+(7*7)+(6*6)+(5*6)+(4*9)+(3*0)+(2*4)+(1*4)=171
171 % 10 = 1
So 176690-44-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO/c14-9-11-4-1-2-6-12(11)10-5-3-7-13-8-10/h1-9H

176690-44-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyridin-3-ylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-PYRIDIN-3-YL-BENZALDEHYDE

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:176690-44-1 SDS

176690-44-1Relevant articles and documents

COMPOUNDS OF PHOSPHINANES AND AZAPHOSPHINANES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

-

Paragraph 0314; 0430; 0431, (2018/02/27)

Compounds of formula (I) wherein: Ak1 represents an alkyl chain, X represents —(CH2)m—, —CH(R)—, —N(R)—, —CH2—N(R)—, —N(R)—CH2— or —CH2—N(R)—CH2—, m and R are as defined in the description, R1 and R2 each represent H when X represents —(CH2)m—, —CH(R)—, —N(R)—, —CH2—N(R)— or —N(R)—CH2—, or together form a bond when X represents —CH2—N(R)—CH2—, R3 represents NH2, Cy-NH2, Cy-Ak3-NH2 or piperidin-4-yl, Cy and Ak3 are as defined in the description, R4 and R5, which may be identical or different, each represent H or F, their optical isomers, and addition salts thereof with a pharmaceutically acceptable acid. Medicinal products containing the same which are useful in treating conditions requiring a TAFIa inhibitor.

Phosphine-Free Suzuki Cross-Coupling Reaction Using an Efficient and Reusable Pd Catalyst in an Aqueous Medium under Microwave Irradiation

Da Silva, Joaquim F. M.,Yepes Perez, Andres F.,De Almeida, Natália P.

supporting information, p. 1995 - 2004 (2015/08/18)

We report here an improved, highly efficient, and general method for the ligand-free Suzuki cross-coupling reaction to the synthesis of biaryls, bipyridyls, thienylpyridine, and allylphenols. Microwave irradiation of (het)aryl halides and (hetaryl, allyl)arylboronic acid N-methyl-iminodiacetic acid (MIDA) ester, using polyurea microencapsulated palladium catalyst (Pd EnCat 30), gave the coupling adducts 1a-x in excellent yields in just 10-18 min.

Cyclometalated Pd(ii) and Ir(iii) 2-(4-bromophenyl)pyridine complexes with N-heterocyclic carbenes (NHCs) and acetylacetonate (acac): Synthesis, structures, luminescent properties and application in one-pot oxidation/Suzuki coupling of aryl chlorides containing hydroxymethyl

Xu, Chen,Li, Hong-Mei,Xiao, Zhi-Qiang,Wang, Zhi-Qiang,Tang, Si-Fu,Ji, Bao-Ming,Hao, Xin-Qi,Song, Mao-Ping

, p. 10235 - 10247 (2014/06/24)

A series of cyclopalladated 2-(4-bromophenyl)pyridine (bpp) complexes [Pd(bpp)(NHC)Cl] 1-3, [Pd(bpp)(acac)] 4, cyclometalated iridium(iii) complexes [Ir(bpp)2Cl]25 and [Ir(bpp)2(acac)] 6 have been synthesized and characterized. Their detailed structures have been determined by X-ray diffraction and many intermolecular C-H...X (Cl, Br, π) and π...π interactions were found in their crystals. Cyclometalated complexes 1-4 and 6 exhibit luminescence with emission peaks of 390-543 nm in dichloromethane solution under UV irradiation. Their application to coupling reactions of aryl chlorides containing hydroxymethyl was also investigated. An efficient 3/Cu cocatalyzed oxidation/Suzuki reaction for the synthesis of biarylaldehydes from chloro-phenylmethanol and arylboronic acids in air has been developed. In addition, a 6/3-cocatalyzed one-pot reaction of acetylferrocene, (2-amino-5-chlorophenyl)methanol, and arylboronic acids provided 6-aryl-2-ferrocenylquinolines in moderate to good yields.

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