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Benzenemethanol, 3-bromo-α-(nitromethyl)-, also known as 3-bromo-α-(nitromethyl)benzenemethanol, is an organic compound with the chemical formula C7H7BrNO2. It is a derivative of benzyl alcohol, featuring a nitromethyl group (-CH2NO2) and a bromine atom (Br) attached to the benzene ring. Benzenemethanol, 3-bromo-a-(nitromethyl)- is characterized by its yellowish color and has potential applications in the synthesis of pharmaceuticals and other organic compounds. Due to the presence of both bromine and nitro groups, it can be involved in various chemical reactions, such as nucleophilic substitutions and redox processes. The compound's properties, such as solubility and reactivity, can be influenced by the electron-withdrawing effects of the nitro group and the electron-donating effects of the benzyl alcohol moiety.

39220-96-7

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39220-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39220-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,2 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39220-96:
(7*3)+(6*9)+(5*2)+(4*2)+(3*0)+(2*9)+(1*6)=117
117 % 10 = 7
So 39220-96-7 is a valid CAS Registry Number.

39220-96-7SDS

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 1-(3-bromophenyl)-2-nitroethanol

1.2 Other means of identification

Product number -
Other names 2-nitro-1-(3-bromophenyl)ethanol

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:39220-96-7 SDS

39220-96-7Upstream product

39220-96-7Relevant academic research and scientific papers

Method for preparing 2-nitroalkyl-1-alcohol compound and application thereof

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Paragraph 0063-0079, (2021/04/14)

The invention relates to a method for preparing a 2-nitroalkane-1-alcohol compound and application thereof, and particularly provides a method for preparing the 2-nitroalkane-1-alcohol compound from iron powder/lead dichloride. The process has the advantages of good yield, high diastereoselectivity, wide functional group tolerance and good compatibility.

Copper-bearing chirality helical coordination polymer and preparation method and application thereof

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Paragraph 0022; 0023; 0024; 0027, (2016/11/21)

The invention discloses a copper-bearing chirality helical coordination polymer and a preparation method and application thereof. The chemical formula is {[Cu (R,R-cdpa) (H2O)2].2NO3. 2H2O}. The preparation method comprises the steps of adding 5 mL of methanol solution into copper dinitrate-water(1/3) and R,R-cdpa to be mixed to obtain suspension liquid and enabling the suspension liquid to stand at room temperature to obtain the copper-bearing chirality helical coordination polymer. The copper-bearing chirality helical coordination polymer has the advantages that a double chelate ligand R,R-cdpa based on chiraity cyclohexanediamine and Cu (II) are utilized to prepare a one-dimensional helical coordination polymer, and the coordination polymer has a right hand 31 helical structure and has second-order non-linear optical activity. The preparing technology is simple, a complex synthesis device is not needed, the production cost is reduced, and the prepared coordination polymer can be applied to asymmetric Henry reaction of aromatic aldehyde and nitromethane.

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