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74447-69-1

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74447-69-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74447-69-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,4 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74447-69:
(7*7)+(6*4)+(5*4)+(4*4)+(3*7)+(2*6)+(1*9)=151
151 % 10 = 1
So 74447-69-1 is a valid CAS Registry Number.

74447-69-1SDS

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 1-bromo-4-(3-methoxyphenyl)benzene

1.2 Other means of identification

Product number -
Other names 1-bromanyl-4-(3-methoxyphenyl)benzene

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:74447-69-1 SDS

74447-69-1Relevant articles and documents

Pyrazole-Mediated C-H Functionalization of Arene and Heteroarenes for Aryl-(Hetero)aryl Cross-Coupling Reactions

Kundu, Abhishek,Dey, Dhananjay,Pal, Subhankar,Adhikari, Debashis

, p. 15665 - 15673 (2021/11/16)

Herein we introduce a transition-metal-free protocol that involves a commercially available, inexpensive pyrazole molecule to conduct C-C cross-coupling reactions at room temperature via a radical pathway. Using this method, an aryldiazonium salt has been coupled to a wide range of arenes and heteroarenes including benzene, mesitylene, thiophene, furan, benzoxazole to result the corresponding biaryl products. The full reaction mechanism is elucidated along with the crystallographic probation of an active initiator species. A potassium-stabilized deprotonated pyrazole steers single-electron transfer to the substrate and behaves as an initiator for the reaction.

Gold-Catalyzed Oxidative Biaryl Cross-Coupling of Organometallics

Liu, Kai,Li, Nian,Ning, Yunyun,Zhu, Chengjian,Xie, Jin

, p. 2718 - 2730 (2019/10/09)

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A process for preparing halogenated biphenyl (by machine translation)

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Paragraph 0029-0030, (2019/05/08)

A process for preparing halogenated biphenyl compound of the method, it is in order to aryl borate and aryl silane reagent as a raw material, 1, 1, 2 - trichloroethane as solvent, oxygenated esters of acetic acid as the oxidizing agent, paratoluene sulfonic acid silver as silver salts. In 110 °C lower, N - (diphenyl phosphate alkyl) - N - isopropyl - 1, 1 - diphenyl phosphine amine [...] 1 a catalytic cross-coupling, and efficient synthesis of aryl compounds of the halogenating is joint method. (by machine translation)

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