Welcome to LookChem.com Sign In|Join Free
  • or
3-(Benzyloxy)-4-methylphenylboronic acid is an organic compound characterized by the chemical formula C14H15BO4. It is a member of the boronic acid class, featuring a boronic acid functional group attached to a benzene ring, which is substituted with a benzyloxy and a methyl group. This white to off-white solid is soluble in common organic solvents such as methanol and dichloromethane, and it plays a significant role in various organic synthesis processes.

1256355-31-3

Post Buying Request

1256355-31-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1256355-31-3 Usage

Uses

Used in Pharmaceutical Synthesis:
3-(Benzyloxy)-4-methylphenylboronic acid is utilized as a key building block in the synthesis of pharmaceuticals. Its unique structure allows for the creation of complex organic molecules that can be used in the development of new drugs.
Used in Agrochemical Production:
In the agrochemical industry, 3-(Benzyloxy)-4-methylphenylboronic acid serves as an essential component in the production of various agrochemicals. Its reactivity and functional group make it suitable for the synthesis of compounds that can be used in crop protection and other agricultural applications.
Used in Organic Synthesis:
3-(Benzyloxy)-4-methylphenylboronic acid is used as a versatile reagent in organic synthesis for the creation of a wide range of organic compounds. Its ability to participate in various chemical reactions makes it a valuable tool in the synthesis of specialty chemicals.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
3-(Benzyloxy)-4-methylphenylboronic acid is employed as a reagent in Suzuki-Miyaura cross-coupling reactions, a type of organic reaction used to form carbon-carbon bonds. This reaction is particularly useful in the synthesis of biologically active compounds and complex organic molecules.
Used in Other Organic Transformations:
Beyond its role in cross-coupling reactions, 3-(Benzyloxy)-4-methylphenylboronic acid is also used in other organic transformations to modify or functionalize organic compounds. Its reactivity and the presence of the boronic acid group make it a useful agent in achieving specific synthetic goals.

Check Digit Verification of cas no

The CAS Registry Mumber 1256355-31-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1256355-31:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*5)+(2*3)+(1*1)=153
153 % 10 = 3
So 1256355-31-3 is a valid CAS Registry Number.

1256355-31-3SDS

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 (3-(Benzyloxy)-4-methylphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names (4-methyl-3-phenylmethoxyphenyl)boronic 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:1256355-31-3 SDS

1256355-31-3Upstream product

1256355-31-3Downstream Products

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1256355-31-3