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475288-40-5

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475288-40-5 Usage

Functional Groups

Thiophene ring, Boronic acid (B(OH)2)

Functional Group Position

Attached to the 7th carbon position of the thiophene ring

Common Uses

Organic synthesis
Building block for pharmaceuticals, agrochemicals, and materials

Applications

Used in cross-coupling reactions
Catalysis

Properties

Boronic acid functionality allows for selective reactions
Unique structure offers versatility in chemical transformations

Significance

Valuable tool for researchers in chemical and pharmaceutical sciences
Enables the development of novel compounds and materials

Check Digit Verification of cas no

The CAS Registry Mumber 475288-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,2,8 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 475288-40:
(8*4)+(7*7)+(6*5)+(5*2)+(4*8)+(3*8)+(2*4)+(1*0)=185
185 % 10 = 5
So 475288-40-5 is a valid CAS Registry Number.

475288-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3-dimethyl-1-benzothiophen-7-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 2,3-Dimethyl-1-benzothien-7-ylboronic 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:475288-40-5 SDS

475288-40-5Downstream Products

475288-40-5Relevant articles and documents

Synthesis using Suzuki cross couplings of sulfur analogues of dehydrotryptophan with a definite stereochemistry

Silva, Natalia O.,Abreu, Ana S.,Ferreira, Paula M. T.,Monteiro, Luis S.,Queiroz, Maria-Joao R. P.

, p. 2524 - 2528 (2007/10/03)

Sulfur analogues of dehydrotryptophan (5-7) were prepared in moderate to good yields (40-80%) by Suzuki cross coupling [Pd(PPh3)4, Na2CO3 or NaHCO3, DME/H2O, 90°C] of several benzo[b]thioph

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