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61593-31-5

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61593-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61593-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,9 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61593-31:
(7*6)+(6*1)+(5*5)+(4*9)+(3*3)+(2*3)+(1*1)=125
125 % 10 = 5
So 61593-31-5 is a valid CAS Registry Number.

61593-31-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(anilinomethyl)-4-bromophenol

1.2 Other means of identification

Product number -
Other names 4-Bromo-2-phenylaminomethyl-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:61593-31-5 SDS

61593-31-5Downstream Products

61593-31-5Relevant articles and documents

Sulfonic acid supported on hydroxyapatite-encapsulated-γ-Fe 2O3 nanocrystallites as a magnetically separable catalyst for one-pot reductive amination of carbonyl compounds

Deng, Jia,Mo, Li-Ping,Zhao, Fei-Yang,Hou, Lan-Lan,Yang, Li,Zhang, Zhan-Hui

experimental part, p. 2576 - 2584 (2011/10/18)

A novel, environmentally friendly procedure has been developed for the preparation of secondary or tertiary amines by one-pot reductive amination of carbonyl compounds using sodium borohydride in the presence of a magnetically recoverable sulfonic acid supported on hydroxyapatite-encapsulated-γ- Fe2O3 [γ-Fe2O3@HAP-SO 3H] at room temperature. The catalyst was easily separated from the reaction mixture by applying an external magnet and reused for six cycles without significant loss of catalytic activity.

Synthesis of new benzoxazaphosphinine/benzoxazaphosphole/ diazaphosphaphenalene-2-sulfides using Lawesson's reagent

Prasad, G. Syam,Babu, B. Hari,Reddy, C. Devendranath,Raju, C. Naga,Reddy, C. Suresh

, p. 85 - 91 (2008/03/14)

Synthesis of new benzoxazaphosphinine/benzoxazaphosphole/ diazaphosphaphenalene 2-sulfides were accomplished by the reaction of Lawesson's reagent (LR) with 4-bromo-2-[(phenylamino) methyl]phenol (1a), 4-bromo-2-[(4-chloro/bromo/methoxy/methylphenyl-amino)methyl]phenol (1b-e), 4-bromo-2-[(benzylamino)methyl]phenol (1f), 2-amino-4-chlorophenol (2a)/2-amino-4-methylphenol (2b), 1,8-diaminonaphthalene (3) respectively in anhydrous toluene. Products 4a-f, 5a-b and 6 were characterized by IR, 1H, 13C, 31P NMR and Mass spectra. Copyright Taylor & Francis Group, LLC.

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