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4-(Methoxycarbonyl)naphthalen-1-ylboronic acid is a boronic acid derivative with the molecular formula C13H11BO4. It features a naphthalene ring with a methoxycarbonyl group attached, making it a versatile building block in organic synthesis. 4-(Methoxycarbonyl)naphthalen-1-ylboronic acid is known for its ability to form stable complexes with diols and is widely utilized in Suzuki coupling reactions for the formation of carbon-carbon bonds. As an important intermediate in organic chemistry, 4-(Methoxycarbonyl)naphthalen-1-ylboronic acid plays a crucial role in the synthesis of complex molecules, particularly in the pharmaceutical and agrochemical industries.

957034-67-2

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957034-67-2 Usage

Uses

Used in Pharmaceutical Industry:
4-(Methoxycarbonyl)naphthalen-1-ylboronic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity enable the development of new drugs with improved efficacy and selectivity. 4-(Methoxycarbonyl)naphthalen-1-ylboronic acid's ability to form stable complexes with diols allows for the creation of drug molecules with enhanced binding properties to their target receptors.
Used in Agrochemical Industry:
In the agrochemical industry, 4-(Methoxycarbonyl)naphthalen-1-ylboronic acid serves as a valuable building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its involvement in Suzuki coupling reactions facilitates the formation of carbon-carbon bonds, leading to the development of novel agrochemicals with increased potency and selectivity.
Used in Organic Synthesis:
4-(Methoxycarbonyl)naphthalen-1-ylboronic acid is used as a versatile building block in organic synthesis for the creation of complex organic molecules. Its reactivity and ability to form stable complexes with diols make it an ideal candidate for the synthesis of a wide range of organic compounds, including natural products, pharmaceuticals, and specialty chemicals.
Used in Suzuki Coupling Reactions:
4-(Methoxycarbonyl)naphthalen-1-ylboronic acid is employed as a reactant in Suzuki coupling reactions, a widely used method for the formation of carbon-carbon bonds. This reaction is particularly useful in the synthesis of biaryl compounds, which are common structural motifs in pharmaceuticals, agrochemicals, and other organic molecules. The use of this boronic acid derivative in Suzuki coupling reactions allows for the efficient and selective formation of these important molecular frameworks.

Check Digit Verification of cas no

The CAS Registry Mumber 957034-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,3 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 957034-67:
(8*9)+(7*5)+(6*7)+(5*0)+(4*3)+(3*4)+(2*6)+(1*7)=192
192 % 10 = 2
So 957034-67-2 is a valid CAS Registry Number.

957034-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxycarbonylnaphthalen-1-yl)boronic acid

1.2 Other means of identification

Product number -
Other names Methyl 4-borononaphthalene-1-carboxylate

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:957034-67-2 SDS

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