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Phenol, 4-cyclohexyl-2-nitro-, also known as 2-Nitro-4-cyclohexylphenol, is an organic compound with the chemical formula C12H15NO3. It is a derivative of phenol, featuring a nitro group at the 2-position and a cyclohexyl group at the 4-position. This yellow crystalline solid is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Due to its reactivity and potential applications, it is essential to handle Phenol, 4-cyclohexyl-2-nitro- with care, as it may pose health and environmental risks.

3279-10-5

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3279-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3279-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,7 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3279-10:
(6*3)+(5*2)+(4*7)+(3*9)+(2*1)+(1*0)=85
85 % 10 = 5
So 3279-10-5 is a valid CAS Registry Number.

3279-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-cyclohexyl-2-nitrophenol

1.2 Other means of identification

Product number -
Other names 4-Cyclohexyl-2-nitro-phenol

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:3279-10-5 SDS

3279-10-5Relevant academic research and scientific papers

Palladium-catalyzed aromatic C-H bond nitration using removable directing groups: Regiospecific synthesis of substituted o -nitrophenols from related phenols

Zhang, Wei,Zhang, Jian,Ren, Shaobo,Liu, Yunkui

, p. 11508 - 11516 (2015/01/09)

A general and regiospecific transformation of substituted phenols into the related o-nitrophenols has been achieved via a three-step process involving the palladium-catalyzed chelation-assisted ortho-C-H bond nitration as the key step. In the process, 2-pyridinyloxy groups act as removable directing groups for the palladium-catalyzed ortho-nitration of substituted 2-phenoxypridines, and they can be readily removed in the subsequent conversion of the resulting 2-(2-nitrophenoxy)pyridines into 2-nitrophenols.

Alkyl-substituted benzoxazinorifamycin derivative, process for preparing the same and antibacterial agent containing the same

-

, (2008/06/13)

A novel rifamycin derivative having the formula (I): STR1 wherein X1 is an alkyl group with 1 to 6 carbon atoms or a cycloalkyl group with 3 to 8 carbon atoms; X2 is a hydrogen atom or an alkyl group with 1 to 4 carbon atoms; R1 is hydrogen atom or acetyl group; A is a group represented by the formula: STR2 wherein R2 is an alkyl group with 1 to 4 carbon atoms or an alkoxyalkyl group with 2 to 6 carbon atoms and R3 is an alkyl group with 1 to 6 carbon atoms or an alkoxyalkyl group with 2 to 6 carbon atoms, or a group represented by the formula STR3 wherein STR4 is a 3 to 9 membered cyclic amino group with 2 to 8 carbon atoms, R4 is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, or salts thereof, a process for preparing the same and antibacterial agents containing the same as an effective ingredient. The rifamycin derivative of the present invention having the formula (I) shows a strong antibacterial activity against the Gram-positive bacteria and the acid-fast bacteria.

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