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4,4-DIAMINO-4-HYDROXYTRIPHENYLMETHANE(DAHTM) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110146-05-9

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110146-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110146-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,1,4 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110146-05:
(8*1)+(7*1)+(6*0)+(5*1)+(4*4)+(3*6)+(2*0)+(1*5)=59
59 % 10 = 9
So 110146-05-9 is a valid CAS Registry Number.

110146-05-9SDS

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 4,4'-diamino-4''-hydroxytriphenylmethane

1.2 Other means of identification

Product number -
Other names 4,4'-DIAMINO-4 -HYDROXYTRIPHENYLMETHANE

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:110146-05-9 SDS

110146-05-9Relevant academic research and scientific papers

Metal- And solvent-free synthesis of aniline- And phenol-based triarylmethanes: Via Br?nsted acidic ionic liquid catalyzed Friedel-Crafts reaction

Jaratjaroonphong, Jaray,Saeeng, Rungnapha,Senapak, Warapong,Sirion, Uthaiwan,ponpao, nipaphorn

, p. 22692 - 22709 (2021/07/21)

A beneficial, scalable and efficient methodology for the synthesis of aniline-based triarylmethanes has been established through the double Friedel-Crafts reaction of commercial aldehydes and primary, secondary or tertiary anilines using Br?nsted acidic ionic liquid as a powerful catalyst, namely [bsmim][NTf2]. This protocol was successfully performed under metal- and solvent-free conditions with a broad range of substrates, giving the corresponding aniline-based triarylmethane products in good to excellent yields (up to 99%). In addition, alternative aromatic nucleophiles such as phenols and electron-rich arenes were also studied using this useful approach to achieve a diversity of triarylmethane derivatives in high to excellent yields. This journal is

Blue light-emitting polyamide and poly(amide-imide)s containing 1,3,4-oxadiazole ring in the side chain

Hamciuc, Corneliu,Hamciuc, Elena,Homocianu, Mihaela,Nicolescu, Alina,Carja, Ionela-Daniela

, p. 110 - 113 (2015/03/31)

A new diamine monomer containing a 1,3,4-oxadiazole ring, 4,4′-diamino-4″-[2-(4-phenoxy)-5-(4-dimethylaminophenyl)-1,3,4-oxadiazole]triphenylmethane, was synthesized and characterized. The diamine is used to prepare novel polyamide and poly(amide-imide)s

Effect of conformational parameters on physical properties of polymers containing pendant phenoxyphthalonitrile substituents

Carja, Ionela-Daniela,Hamciuc, Corneliu,Vlad-Bubulac, Tachita,Bruma, Maria,Ronova, Inga A.

, p. 1693 - 1703 (2013/10/22)

Heteroaromatic polymers are considered to be high performance organic materials due to their unique and highly attractive properties, including outstanding thermal and mechanical resistance, that arise from their aromatic structure and strong interactions

Microwave-assisted synthesis of 4,4′-diaminotriphenylmethanes

Guzmán-Lucero,Guzmán,Likhatchev,Martínez-Palou

, p. 1119 - 1122 (2007/10/03)

A fast, efficient and versatile route of synthesis of 4,4′- diaminotriphenylmethanes under microwave irradiation, suitable for parallel library syntheses were developed.

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