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289032-37-7

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289032-37-7 Usage

Also known as

benzhydryl valeraldehyde

Classification

aromatic aldehyde

Mains uses

fragrance and flavoring agent, production of synthetic flavors and perfumes

Odor

strong, sweet, floral, jasmine-like

Additional uses

reagent in organic synthesis, formulation of various chemical products

Regulation

due to potential health and environmental hazards

Check Digit Verification of cas no

The CAS Registry Mumber 289032-37-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,0,3 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 289032-37:
(8*2)+(7*8)+(6*9)+(5*0)+(4*3)+(3*2)+(2*3)+(1*7)=157
157 % 10 = 7
So 289032-37-7 is a valid CAS Registry Number.

289032-37-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-phenylphenyl)pentanal

1.2 Other means of identification

Product number -
Other names 5-(4-BIPHENYLYL)PENTANAL

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:289032-37-7 SDS

289032-37-7Downstream Products

289032-37-7Relevant articles and documents

Rhodium-Catalyzed Remote C(sp3)?H Borylation of Silyl Enol Ethers

Li, Jie,Qu, Shuanglin,Zhao, Wanxiang

supporting information, p. 2360 - 2364 (2020/01/02)

A rhodium-catalyzed remote C(sp3)?H borylation of silyl enol ethers (SEEs, E/Z mixtures) by alkene isomerization and hydroboration is reported. The reaction exhibits mild reaction conditions and excellent functional-group tolerance. This method is compatible with an array of SEEs, including linear and branched SEEs derived from aldehydes and ketones, and provides direct access to a broad range of structurally diverse 1,n-borylethers in excellent regioselectivities and good yields. These compounds are precursors to various valuable chemicals, such as 1,n-diols and aminoalcohols.

DESIGN AND SYNTHESIS OF OPTIMIZED LIGANDS FOR PPAR

-

Page/Page column 34, (2010/02/10)

This invention provides new chemical entities useful for treating a variety of clinical disorders including those that areinfluenced by the activity of peroxisome proliferator activated receptors (PPAR). The structures of the compounds and methods to design, make and use the compounds are provided. Compounds and methods for administering therapeutic compositions comprising the compounds in cases of the disease psoriasis are provided. An exemplary compound having the formula compound is 5-adamantan-2-yl-pentanoic acid {2-[4-(2,4-dioxo-thiazolidin-5-yl-methyl)-phenoxy]-ethyl}-methyl-amide is provided.

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