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3155-01-9

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3155-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3155-01-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3155-01:
(6*3)+(5*1)+(4*5)+(3*5)+(2*0)+(1*1)=59
59 % 10 = 9
So 3155-01-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-8(11)10(2,12)9-6-4-3-5-7-9/h3-7,12H,1-2H3

3155-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-3-phenylbutan-2-one

1.2 Other means of identification

Product number -
Other names 3-hydroxy-3-phenyl-2-butanone

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:3155-01-9 SDS

3155-01-9Relevant articles and documents

Novel routes to N-amino-1H-pyrrolo[2,3-b]pyridines from α-hydroxyarylalkyl ketones and hydrazines

Chudinov,Gashev,Firgang,Semenov

, p. 1612 - 1616 (2007)

Treatment of 3-hydroxy-3-(3-pyridyl)butan-2-one hydrazone with polyphosphoric acid gave 1-amino-2,3-dimethyl-1H-pyrrolo[2,3-b]pyridine. An analogous reaction with 2,4-dinitrophenylhydrazone of the same ketone yielded 1-(2,4-dinitrophenyl)-3-methyl-4-(3-pyridyl)pyrazole.

ELECTRO-OPTIC POLYMER

-

Paragraph 0150-0153; 162, (2021/02/05)

The present invention provides an electro-optic polymer (EO polymer) comprising an electro-optic molecule (EO molecule) and a base polymer. The EO polymer of the present invention has good performance over the entire optical communication wavelength range

D-π-A chromophores with a quinoxaline core in the π-bridge and bulky aryl groups in the acceptor: Synthesis, properties, and femtosecond nonlinear optical activity of the chromophore/PMMA guest-host materials

Balakina, Marina Yu,Budnikova, Yulia H.,Dudkina, Yulia B.,Fazleeva, Guzel M.,Fominykh, Olga D.,Islamova, Liliya N.,Kalinin, Alexey A.,Khamatgalimov, Ayrat R.,Levitskaya, Alina I.,Mukhtarov, Anvar S.,Nizameev, Irek R.,Sharipova, Anastasiya V.,Shmelev, Artemiy G.,Vakhonina, Tatyana A.

, (2020/09/04)

Novel D-π-A chromophores with quinoxaline/quinoxalinone core in the π-conjugated bridge and various bulky groups in the acceptor moiety have been synthesized and systematically investigated at molecular level by UV–Vis spectroscopy, DFT calculations, electrochemical and TGA-DSC methods as well as at materials level by the example of PMMA-based composite polymer materials doped with different chromophore contents using molecular modeling and SHG technique. Chromophores exhibit positive dioxane/chloroform solvatochromic shift of ca. 50 nm, high values of first hyperpolarizability and dipole moment, small energy gap and good thermal stability. Tolyl and cyclohexylphenyl substituents unlike phenyl can be treated as most effective isolating groups, preventing chromophore pronounced aggregation even at 30 wt% content. Femtosecond nonlinear optical (NLO) activity was studied for poled thin guest-host polymer films with various chromophore weight content. Film DBA-VQPhV-TCFPhCy(25 wt%)/PMMA with bulky cyclohexylphenyl groups in chromophore acceptor shows maximal NLO coefficient, d33, values among the studied materials (37 pm/V) as well as good long-term stability of NLO response together with excellent chromophore thermal stability (Td = 256 °C). Composite materials doped with quinoxaline chromophores are photostable with respect to laser pulses with peak intensities up to 11 GW/cm2.

A CO2-mediated base catalysis approach for the hydration of triple bonds in ionic liquids

Han, Buxing,Ke, Zhengang,Li, Ruipeng,Liu, Zhimin,Tang, Minhao,Wang, Yuepeng,Zeng, Wei,Zhang, Fengtao,Zhao, Yanfei

supporting information, p. 9870 - 9875 (2021/12/27)

Herein, we report a CO2-mediated base catalysis approach for the activation of triple bonds in ionic liquids (ILs) with anions that can chemically capture CO2 (e.g., azolate, phenolate, and acetate), which can achieve hydration of triple bonds to carbonyl chemicals. It is discovered that the anion-complexed CO2 could abstract one proton from proton resources (e.g., IL cation) and transfer it to the CN or CC bonds via a six-membered ring transition state, thus realizing their hydration. In particular, tetrabutylphosphonium 2-hydroxypyridine shows high efficiency for hydration of nitriles and CC bond-containing compounds under a CO2 atmosphere, affording a series of carbonyl compounds in excellent yields. This catalytic protocol is simple, green, and highly efficient and opens a new way to access carbonyl compounds via triple bond hydration under mild and metal-free conditions.

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