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58452-00-9

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58452-00-9 Usage

Uses

3-Benzyloxy-4-methoxybenzoic acid is used as Pharmaceutical intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 58452-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,5 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58452-00:
(7*5)+(6*8)+(5*4)+(4*5)+(3*2)+(2*0)+(1*0)=129
129 % 10 = 9
So 58452-00-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O4/c1-18-13-8-7-12(15(16)17)9-14(13)19-10-11-5-3-2-4-6-11/h2-9H,10H2,1H3,(H,16,17)

58452-00-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L05731)  3-Benzyloxy-4-methoxybenzoic acid, 97+%   

  • 58452-00-9

  • 1g

  • 391.0CNY

  • Detail
  • Alfa Aesar

  • (L05731)  3-Benzyloxy-4-methoxybenzoic acid, 97+%   

  • 58452-00-9

  • 5g

  • 1393.0CNY

  • Detail
  • Alfa Aesar

  • (L05731)  3-Benzyloxy-4-methoxybenzoic acid, 97+%   

  • 58452-00-9

  • 25g

  • 5572.0CNY

  • Detail

58452-00-9SDS

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-methoxy-3-phenylmethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 3-benzyloxy-p-anisic 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:58452-00-9 SDS

58452-00-9Relevant articles and documents

COMPLEMENT MODULATORS AND RELATED METHODS

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Paragraph 0388, (2020/10/20)

The present disclosure presents compounds and compositions that interact with complement components. Some compounds inhibit complement activity. Included are small molecule compounds and compositions that function as C5 inhibitor compounds. Methods for inhibiting complement activity and methods of treating complement-related indications with the C5 inhibitor compounds and compositions are provided.

With anti-tumor activity of the benzamide compound and its preparation method and application

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Paragraph 0043-0044, (2017/03/08)

The invention discloses a benzamide compound with antitumor activity as well as a preparation method and application thereof. The structural formula of the compound is shown in the specification, wherein in the structural formula, R1 is hydrogen or halogen; R2 is alkoxy with carbon number of 1-4; the terminal of R2 is replaced by tert-amido; R2 is linked to the para-position of benzamide via oxygen atoms; R3 is one of hydroxyl or methoxyl; R4 is the other one of hydroxyl or methoxyl. The compound has good tumor cell inhibiting activity in vitro and can be used for preparing antitumor drugs, especially anti-hepatoma drugs and anti-breast cancer drugs. The preparation method of the benzamide compound, provided by the invention, has the advantages that the raw materials are accessible, the reaction conditions are mild, the reaction process is simple to operate, and the used reagent is cheap.

NOVEL GLYCOSYLTRANSFERASE, NOVEL GLYCOSYLTRANSFERASE GENE, AND NOVEL GLYCOSYL DONOR COMPOUND

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Paragraph 0106, (2015/09/22)

An object of the present invention is to provide a sugar donating reagent comprising a sugar donor compound other than a sugar nucleotide and an enzyme capable of catalyzing a glycosyl transfer reaction using a sugar donor compound other than a sugar nucleotide. The present invention provides the following: a sugar donating reagent containing a compound of formula (A): wherein R 1 is independently selected from hydrogen, or C 1-6 alkyl, C 2-6 alkenyl, and C 2-6 alkynyl in which each of the groups is unsubstituted or substituted with one or more groups selected from OH, F, Cl, Br, I, CN, NO 2 , and SO 2 , n is 0, 1, 2, 3, 4 or 5, m is 0 or 1, and X represents a monosaccharide bound via a 2 bond on its anomeric carbon; a glycosyltransferase capable of catalyzing a glycosyl transfer reaction using the sugar donor; and a glycosyltransferase gene comprising DNA encoding the glycosyltransferase.

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