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40295-80-5

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40295-80-5 Usage

General Description

1-(2-Naphthyl)ethanol is a chemical compound with the molecular formula C12H12O. It is a white or off-white crystalline solid with a faint odor, and it is insoluble in water but soluble in organic solvents. 1-(2-Naphthyl)ethanol is commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds. It is also utilized in the production of fragrances, perfumes, and flavorings. Additionally, it has been studied for its potential therapeutic properties, including anti-inflammatory and anti-tumor activities. However, further research is needed to fully understand the potential uses and effects of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 40295-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,9 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40295-80:
(7*4)+(6*0)+(5*2)+(4*9)+(3*5)+(2*8)+(1*0)=105
105 % 10 = 5
So 40295-80-5 is a valid CAS Registry Number.

40295-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-?Naphthalenemethanol, α-?methyl-

1.2 Other means of identification

Product number -
Other names -

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:40295-80-5 SDS

40295-80-5Downstream Products

40295-80-5Relevant articles and documents

Asymmetric transfer hydrogenation of prochiral ketones in aqueous media with new water-soluble chiral vicinal diamine as ligand

Ma, Yaping,Liu, Hui,Chen, Li,Cui, Xin,Zhu, Jin,Deng, Jingen

, p. 2103 - 2106 (2007/10/03)

(Matrix presented) An easily accessible water-soluble chiral o-sulfonated 1,2-diphenylethlenediamine 2 and its mono-N-tosylated derivative 3 were synthesized for the first time. The ruthenium-complex-catalyzed reduction of prochiral ketones in aqueous media has been examined by using 3 as ligand and sodium formate as the source of hydrogen. The asymmetric transfer hydrogenation of ω-bromo acetophenones was achieved, in which only formate displacement occurred when formic acid/triethylamine azeotrope was used as the hydrogen donor.

Irreversible and Highly Enantioselective Acylation of 2-Halo-1-arylethanols in Organic Solvents Catalyzed by a Lipase from Pseudomonas fluorescens

Hiratake, Jun,Inagaki, Minoru,Nishioka, Takaaki,Oda, Jun'ichi

, p. 6130 - 6133 (2007/10/02)

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