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4,4'-Dimethoxybiphenyl-2,2'-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54147-88-5

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54147-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54147-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,4 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54147-88:
(7*5)+(6*4)+(5*1)+(4*4)+(3*7)+(2*8)+(1*8)=125
125 % 10 = 5
So 54147-88-5 is a valid CAS Registry Number.

54147-88-5SDS

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 4,4'-dimethoxy-biphenyl-2,2'-diyldiamine

1.2 Other means of identification

Product number -
Other names 2.2'-Diamino-4.4'-dimethoxy-biphenyl

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:54147-88-5 SDS

54147-88-5Relevant academic research and scientific papers

Synthesis of Unexpected trans-meso Macrocycle from Novel Unsymmetrical Tetraphenylene

Deng, Chun-Lin,Hau, Sam C. K.,Peng, Xiao-Shui,Wong, Henry N. C.

, p. 2095 - 2100 (2016)

A highly unsymmetrical trisubstituted tetraphenylene was designed and synthesized as a novel superamolecular scaffold for an unexpected trans-meso tetraphenylene macrocycle, whose structure was unequivocally characterized by an X-ray crystallographic anal

Visible-Light-Induced Synthesis of Carbazoles by in Situ Formation of Photosensitizing Intermediate

Chatterjee, Tanmay,Roh, Geum-Bee,Shoaib, Mahbubul Alam,Suhl, Chang-Heon,Kim, Jun Soo,Cho, Cheon-Gyu,Cho, Eun Jin

supporting information, p. 1906 - 1909 (2017/04/11)

A visible-light-induced synthesis of N-H carbazoles from easily accessible 2,2′-diaminobiaryls in the absence of any external photosensitizer is reported. The process only requires tBuONO and natural resources, visible light, and molecular oxygen for the synthesis of N-H carbazoles. Experimental and computational studies support that the in situ formation of a visible-light-absorbing photosensitizing intermediate, benzocinnoline N-imide, is responsible for the activation of triplet molecular oxygen to singlet oxygen that, in turn, promotes the synthesis of carbazole.

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