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151588-38-4

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151588-38-4 Usage

General Description

4-BUTYLTHIOPHENYLBORONIC ACID is a chemical compound with the formula C10H13BO2S. It is a boronic acid derivative containing a butylthiophene group, which makes it a useful building block in organic synthesis for various applications. 4-BUTYLTHIOPHENYLBORONIC ACID is commonly used in the pharmaceutical and agrochemical industries as a reagent for the synthesis of biologically active compounds. It is also utilized in the development of organic electronic materials and as a ligand in metal-catalyzed coupling reactions. 4-BUTYLTHIOPHENYLBORONIC ACID is considered a versatile and important chemical for the preparation of various functionalized molecules and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 151588-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,5,8 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 151588-38:
(8*1)+(7*5)+(6*1)+(5*5)+(4*8)+(3*8)+(2*3)+(1*8)=144
144 % 10 = 4
So 151588-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H15BO2S/c1-2-3-8-14-10-6-4-9(5-7-10)11(12)13/h4-7,12-13H,2-3,8H2,1H3

151588-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Butylthiophenylboronic acid

1.2 Other means of identification

Product number -
Other names 4-BUTYLTHIOPHENYLBORONIC ACID

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:151588-38-4 SDS

151588-38-4Relevant articles and documents

Boosting the Charge Transport Property of Indeno[1,2-b]fluorene-6,12-dione though Incorporation of Sulfur- or Nitrogen-Linked Side Chains

Fan, Zhi-Ping,Li, Xiang-Yang,Luo, Xiao-E.,Fei, Xian,Sun, Bing,Chen, Li-Chuan,Shi, Zi-Fa,Sun, Chun-Lin,Shao, Xiangfeng,Zhang, Hao-Li

, (2017/10/12)

Alkyl chains are basic units in the design of organic semiconductors for purposes of enhancing solubility, tuning electronic energy levels, and tailoring molecular packing. This work demonstrates that the carrier mobilities of indeno[1,2-b]fluorene-6,12-d

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