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177665-49-5

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177665-49-5 Usage

General Description

2-(3-(Hydroxymethyl)phenyl)acetonitrile is a chemical compound with the molecular formula C9H9NO. It is a derivative of acetonitrile and features a phenyl ring bearing a hydroxymethyl functional group at the 3-position. This chemical is commonly used in organic synthesis and pharmaceutical research as a building block for more complex molecules. It is also known for its potential application as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, it may have various industrial uses as a reactant in chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 177665-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,6,6 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 177665-49:
(8*1)+(7*7)+(6*7)+(5*6)+(4*6)+(3*5)+(2*4)+(1*9)=185
185 % 10 = 5
So 177665-49-5 is a valid CAS Registry Number.

177665-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-(hydroxymethyl)phenyl]acetonitrile

1.2 Other means of identification

Product number -
Other names 3-Oxymethyl-phenylessigsaeurenitril

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:177665-49-5 SDS

177665-49-5Relevant articles and documents

SEPIAPTERIN REDUCTASE INHIBITORS FOR THE TREATMENT OF PAIN

-

, (2011/05/05)

Disclosed herein are small molecule heterocyclic inhibitors of sepiapterin reductase (SPR), and pro-drugs and pharmaceutically acceptable salts thereof. The Also featured are pharmaceutical compositions of the compounds and uses of these compounds for the treatment or prevention of pain (e.g., inflammatory pain, nociceptive pain, functional pain, and neuropathic pain)

Nucleophilic de-coordination and electrophilic regeneration of "hemilabile" pincer-type complexes: Formation of anionic dialkyl, diaryl, and dihydride PtII complexes bearing no stabilizing π-acceptors

Poverenov, Elena,Gandelman, Mark,Shimon, Linda J. W.,Rozenberg, Haim,Ben-David, Yehoshoa,Milstein, David

, p. 4673 - 4684 (2007/10/03)

Novel anionic dialkyl, diaryl, and dihydride platinum(II) complexes based on the new πlong-armπ hemilabile PCN-type ligand C6H 4[CH2P(tBu)2](CH2) 2N(CH3)2 with the general formula Li + [Pt(PCN)(R)2]- (R = Me (4), Ph (6) and H (9)) were prepared by reaction of [Pt(PCN)(R)] complexes (obtained from the corresponding chlorides) with an equivalent of RLi, as a result of the opening of the chelate ring. Alkylating agents based on other metals produce less stable products. These anionic d8 complexes are thermally stable although they bear no stabilizing π acceptors. They were characterized by 1H, 31P{1H}, 13C, and 7Li NMR spectroscopy; complex 9 was also characterized by single crystal X-ray crystallography, showing that the Li + ion is coordinated to the nitrogen atom of the open amine arm and to the hydride ligand (trans to the P atom) of a neighboring molecule (H-Li = 2.15 A), resulting in a dimeric structure. Complexes 4 and 9 exhibit high nucleophilic reactivity, upon which the pincer complex is regenerated. Reaction of 4 with water, methyl iodide, and iodobenzene resulted in the neutral complex [Pt(PCN)(CH3)] (3) and methane, ethane, or toluene, respectively. Labeling studies indicate that the reaction proceeds by direct electrophilic attack on the metal center, rather than attack on the alkyl ligand. The anionic dihydride complex 9 reacted with water and methyl iodide to yield [Pt(PCN)(H)] (8) and H2 or methane, respectively.

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