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1877-71-0

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1877-71-0 Usage

Chemical Properties

White to off-white crystalline powder

Uses

Different sources of media describe the Uses of 1877-71-0 differently. You can refer to the following data:
1. Exploited in the synthesis of polymer films.1
2. Exploited in the synthesis of polymer films.

Check Digit Verification of cas no

The CAS Registry Mumber 1877-71-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,7 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1877-71:
(6*1)+(5*8)+(4*7)+(3*7)+(2*7)+(1*1)=110
110 % 10 = 0
So 1877-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O4/c1-13-9(12)7-4-2-3-6(5-7)8(10)11/h2-5H,1H3,(H,10,11)

1877-71-0 Well-known Company Product Price

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

  • (L12992)  Methyl hydrogen isophthalate, 97%   

  • 1877-71-0

  • 1g

  • 443.0CNY

  • Detail
  • Alfa Aesar

  • (L12992)  Methyl hydrogen isophthalate, 97%   

  • 1877-71-0

  • 5g

  • 1473.0CNY

  • Detail

1877-71-0SDS

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 3-methoxycarbonylbenzoic acid

1.2 Other means of identification

Product number -
Other names Isophthalic Acid Monomethyl Ester

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:1877-71-0 SDS

1877-71-0Relevant articles and documents

An efficient and scalable synthesis of methyl 3-hydroxymethylbenzoate

Chen,Davidson,Freisler,Iakovleva,Magano

, p. 381 - 384 (2000)

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Detoxification of VX and Other V-Type Nerve Agents in Water at 37 °C and pH 7.4 by Substituted Sulfonatocalix[4]arenes

Schneider, Christian,Bierwisch, Anne,Koller, Marianne,Worek, Franz,Kubik, Stefan

, p. 12668 - 12672 (2016)

Sulfonatocalix[4]arenes with an appended hydroxamic acid residue can detoxify VX and related V-type neurotoxic organophosphonates with half-lives down to 3 min in aqueous buffer at 37 °C and pH 7.4. The detoxification activity is attributed to the millimo

Silica-Mediated Monohydrolysis of Dicarboxylic Esters

Dyker, Gerald

supporting information, p. 6773 - 6776 (2021/12/31)

A new method for the monohydrolysis of dicarboxylic esters is presented, involving as key step a silanolysis at elevated temperatures at the silica gel surface. In the second step, the surface bound silyl esters are cleaved off under mild conditions, giving a straightforward and fast access to half esters. Based on recovered starting material generally yields well above 70 % are achieved, both, with stiff aromatic as well as flexible aliphatic substrates, as long as the ester groups involved are remote enough from each other. Otherwise competing reactions are becoming determinative, anhydride formation in the case of phthalates and decarbonylative fragmentation in the case of malonates. The new method was also successfully tested on a multigram scale with a minimalistic apparatus setup.

Cobalt-Catalyzed Deprotection of Allyl Carboxylic Esters Induced by Hydrogen Atom Transfer

Li, Nan,Gui, Yizhen,Chu, Mengqi,You, Mengdi,Qiu, Xiaohan,Liu, Hejia,Wang, Shiang,Deng, Meng,Ji, Baoming

supporting information, p. 8460 - 8464 (2021/11/13)

A brief, efficient method has been developed for the removal of the allyl protecting group from allyl carboxylic esters using a Co(II)/TBHP/(Me2SiH)2O catalytic system. This facile strategy displays excellent chemoselectivity, functional group tolerance, and high yields. This transformation probably occurs through the hydrogen atom transfer process, and a Co(III)-six-membered cyclic intermediate is recommended.

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