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2-Nitro-1,1-diphenylethanol is an organic compound with the chemical formula C14H13NO3. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and ether. 2-nitro-1,1-diphenylethanol is characterized by the presence of a nitro group (-NO2) at the 2-position, a hydroxyl group (-OH) at the 1-position, and two phenyl rings attached to the central carbon atom. 2-Nitro-1,1-diphenylethanol is synthesized through various chemical reactions, such as the nitration of 1,1-diphenylethanol or the reduction of 2-nitro-1,1-diphenylethanone. It has potential applications in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds due to its unique structural features.

7475-15-2

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7475-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7475-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7475-15:
(6*7)+(5*4)+(4*7)+(3*5)+(2*1)+(1*5)=112
112 % 10 = 2
So 7475-15-2 is a valid CAS Registry Number.

7475-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-1,1-diphenylethanol

1.2 Other means of identification

Product number -
Other names 2-Nitro-1,1-diphenyl-aethanol

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:7475-15-2 SDS

7475-15-2Relevant academic research and scientific papers

Oxidative nitration of alkenes with tert-butyl nitrite and oxygen

Taniguchi, Tsuyoshi,Yajima, Atsushi,Ishibashi, Hiroyuki

supporting information; experimental part, p. 2643 - 2647 (2011/11/30)

A method for the oxidative nitration of alkenes using a combination of tert-butyl nitrite and molecular oxygen to give β-nitro alcohols and their nitrate derivatives has been developed. The present reaction provides a practical method for the synthesis of

FORMATION OF NITRO COMPOUNDS DURING THE NITROSATION OF OLEFINS BY ALKYL NITRITES

Yandovskii, V. N.,Ryabinkin, I. I.,Tselinskii, I. V.

, p. 1773 - 1775 (2007/10/02)

Vicinal nitro alcohols and/or dinitro derivatives are formed in the reaction of olefins containing a quaternary carbon atom with alkyl nitrites in acetic acid.

Reduction of 2,2-Diaryl-1-nitroethylenes : New Synthesis of 2,2-Diarylacetaldehydes and 1,1,4,4-Tetraarylbuta-1,3-dienes

Tadros, Wadie,Awad, Sami B.,Sakla, Alfy B.,Abdul-Malik, Nadia F.,Armanious, Emili R.

, p. 199 - 202 (2007/10/02)

2,2-Diarylacetaldehydes (VII) have been obtained by selective and controlled reduction of 2,2-diaryl-1-nitroethylenes (IV) in acid medium, and also by acid hydrolysis of 2,2-diarylvinyl-N-acetamides (VI).Nitroalkenes (IV) have been prepared by the reaction of 2,2-diarylethylenes (I) with nitrous acid whereas N-acetamide derivatives (VI) have been obtained by reductive acetylation of the nitro compounds (IV).A number of 1,1,4,4-tetraarylbuta-1,3-dienes (XI) have been obtained by the condensation of 2,2-diarylacetaldehydes (VII) with appropriate 2,2-diarylethylenes (I).Structures of the products have been assigned on the basis of analytical data and chemical and spectral evidences.

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