Welcome to LookChem.com Sign In|Join Free

CAS

  • or

496-14-0

Post Buying Request

496-14-0 Suppliers

Recommended suppliersmore

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

496-14-0 Usage

Description

Phthalan, also known as 2,3-dihydrobenzofuran, is a benzofuran compound that plays a significant role in various organic reactions. It is characterized by its unique structure and reactivity, making it a valuable intermediate in the synthesis of various organic compounds.

Uses

Used in Organic Synthesis:
Phthalan is used as an intermediate in the synthesis of various organic compounds, including tetrahydroquinolines and isochromans. Its reactivity allows for the arylation of these compounds, leading to the formation of new and diverse chemical structures.
Used in Benzylic C-H Bond Activation:
Phthalan is also used in the oxidation and amination of benzylic sp3 C-H bonds. This allows for the functionalization of benzylic positions, enabling the synthesis of a wide range of organic compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 496-14-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 496-14:
(5*4)+(4*9)+(3*6)+(2*1)+(1*4)=80
80 % 10 = 0
So 496-14-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O/c1-2-4-8-6-9-5-7(8)3-1/h1-4H,5-6H2

496-14-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (45592)  Phthalan, 96%   

  • 496-14-0

  • 5g

  • 195.0CNY

  • Detail
  • Alfa Aesar

  • (45592)  Phthalan, 96%   

  • 496-14-0

  • 25g

  • 790.0CNY

  • Detail
  • Alfa Aesar

  • (45592)  Phthalan, 96%   

  • 496-14-0

  • 100g

  • 2378.0CNY

  • Detail
  • Alfa Aesar

  • (A10217)  Phthalan, 98%   

  • 496-14-0

  • 5g

  • 513.0CNY

  • Detail
  • Alfa Aesar

  • (A10217)  Phthalan, 98%   

  • 496-14-0

  • 25g

  • 1075.0CNY

  • Detail
  • Alfa Aesar

  • (A10217)  Phthalan, 98%   

  • 496-14-0

  • 100g

  • 3693.0CNY

  • Detail
  • Aldrich

  • (176877)  Phthalan  97%

  • 496-14-0

  • 176877-5G

  • 560.43CNY

  • Detail

496-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Dihydroisobenzofuran

1.2 Other means of identification

Product number -
Other names Phthalan

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:496-14-0 SDS

496-14-0Relevant articles and documents

Improved Synthesis of 1-Ethoxy-1,3-dihydroisobenzofuran, a Useful Precursor to Isobenzofuran

Moss, Randall J.,Rickborn, Bruce

, p. 5391 - 5393 (1982)

-

Catalytic reductive deoxygenation of esters to ethers driven by hydrosilane activation through non-covalent interactions with a fluorinated borate salt

Agbossou-Niedercorn, Francine,Dixit, Ruchi,Merle, Nicolas,Michon, Christophe,Rysak, Vincent,Trivelli, Xavier,Vanka, Kumar

, p. 4586 - 4592 (2020/08/14)

We report the catalytic and transition metal-free reductive deoxygenation of esters to ethers through the use of a hydrosilane and a fluorinated borate BArF salt as a catalyst. Experimental and theoretical studies support the role of noncovalent interactions between the fluorinated catalyst, the hydrosilane and the ester substrate in the reaction mechanism.

An ether compound of green high-efficient synthetic method (by machine translation)

-

Paragraph 0051, (2018/07/07)

The invention discloses an ether compound of green high-efficient synthetic method, energy-saving environmental protection, comprising: mild reaction system, uses aldehyde, silane as the starting material, under the action of the silver salt in a price, for in solvent-free conditions, through reducing the - coupling - cheng mi reaction, realization of high efficiency alcohol of preparation. Synthesis method of the invention has the advantages of low dosage of catalyst, solvent-free, conversion and high yield, the reaction time is short, safe and stable, easy to operate, the product only distillation purification without any additional organic solvent, the whole range of green, environmental protection, high efficiency and the like, can overcome the defects of the prior art, it has very good industrial application value. (by machine translation)

Synthesis of five- and six-membered heterocycles by dimethyl carbonate with catalytic amounts of nitrogen bicyclic bases

Aricò,Evaristo,Tundo

, p. A1176 - A1185 (2015/03/04)

A catalytic amount of a nitrogen bicyclic base, i.e., DABCO, DBU or TBD, is effective for the one-pot synthesis of heterocycles from 1,4-, 1,5-diols and 1,4-bifunctional compounds via dimethyl carbonate chemistry under neat conditions. Nitrogen bicyclic bases that were previously shown to have enhanced the reactivity of DMC in methoxycarbonylation reaction by a BAc2 mechanism are herein used for the first time as efficient catalysts for cyclization reactions encompassing both BAc2 and BAl2 pathways. This synthesis procedure was also applied to a large scale synthesis of cyclic sugars, isosorbide and isomannide, starting from d-sorbitol and d-mannitol, respectively. The resulting anhydro sugar alcohols were obtained as pure crystalline compounds that did not require any further purification or crystallization. This journal is

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

What can I do for you?
Get Best Price

Get Best Price for 496-14-0