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3339-82-0

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3339-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3339-82-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3339-82:
(6*3)+(5*3)+(4*3)+(3*9)+(2*8)+(1*2)=90
90 % 10 = 0
So 3339-82-0 is a valid CAS Registry Number.

3339-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-(2,2'-bithiophen)-5'-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names 5-Brom-5'-methoxycarbonyl-2,2'-bithienyl

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:3339-82-0 SDS

3339-82-0Downstream Products

3339-82-0Relevant articles and documents

Pd-catalyzed oxidative cross-coupling between two electron rich heteroarenes

He, Chun-Yang,Wang, Zhen,Wu, Cai-Zhi,Qing, Feng-Ling,Zhang, Xingang

, p. 3508 - 3513 (2013)

The transition-metal-catalyzed oxidative cross-coupling between two coupling partners with similar structure and electronic characteristics remains a challenge owing to difficulty in suppressing undesired homo-couplings. We herein report a Pd-catalyzed oxidative cross-coupling between two thiophenes under mild reaction conditions. This approach can also be extended to furans. Some notable advantages of this reaction lie in its synthetic simplicity with the omission of the toxic stannanes coupling partner and excellent functional-group compatibility. The features of this protocol make it an ideal strategy for the construction of a 2,2′-thiophene-thiophene linkage of interest in electronic and optoelectronic materials.

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