Cas 1365531-20-9,5-adamantan-1-yl-N-(2,4-dihydroxybenzyl)-2-hydroxy-4-methoxy-benzoic acid amide

1365531-20-9

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Basic information

Product Name: 5-adamantan-1-yl-N-(2,4-dihydroxybenzyl)-2-hydroxy-4-methoxy-benzoic acid amide
Synonyms: 5-adamantan-1-yl-N-(2,4-dihydroxybenzyl)-2-hydroxy-4-methoxy-benzoic acid amide
CAS NO:1365531-20-9
Molecular Formula:
Molecular Weight: 423.509
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-adamantan-1-yl-N-(2,4-dihydroxybenzyl)-2-hydroxy-4-methoxy-benzoic acid amide(CAS DataBase Reference)
NIST Chemistry Reference: 5-adamantan-1-yl-N-(2,4-dihydroxybenzyl)-2-hydroxy-4-methoxy-benzoic acid amide(1365531-20-9)
EPA Substance Registry System: 5-adamantan-1-yl-N-(2,4-dihydroxybenzyl)-2-hydroxy-4-methoxy-benzoic acid amide(1365531-20-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1365531-20-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1365531-20-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,5,3 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1365531-20:
(9*1)+(8*3)+(7*6)+(6*5)+(5*5)+(4*3)+(3*1)+(2*2)+(1*0)=149
149 % 10 = 9
So 1365531-20-9 is a valid CAS Registry Number.

1365531-20-9Upstream product

1365531-20-9Downstream Products

1365531-20-9Relevant academic research and scientific papers

METHOD FOR PREPARING BENZOIC ACID AMIDE COMPOUND

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Paragraph 0113-0116; 0120-0121, (2018/07/15)

The present invention relates to a method for preparing a benzoic acid amide compound in a high yield by presenting a novel method for preparing a benzyl amine compound to be used as a reactant and delimiting the reaction condition of each step by using the same, and the method is economically advantageous since mass production is possible.

NOVEL BENZOIC ACID AMIDE COMPOUND

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Paragraph 0046; 0070, (2014/06/24)

The present invention relates to a novel benzoic acid amide derivative compound, isomers thereof, pharmaceutically acceptable salts thereof, prodrugs thereof, hydrates thereof, or solvates thereof. The novel compound has excellent skin whitening effects.

NOVEL BENZOIC ACID AMIDE COMPOUND

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Paragraph 0065; 0071; 0089, (2014/09/03)

3D-QSAR study of adamantyl N-benzylbenzamides as melanogenesis inhibitors

Hong, Yong Deog,Baek, Heung Soo,Cho, Haelim,Ahn, Soo Mi,Rho, Ho Sik,Park, Young-Ho,Joo, Yung Hyup,Shin, Song Seok

, p. 667 - 673 (2014/01/23)

Three-dimensional quantitative structure-activity relationship (3D-QSAR) modeling, comparative molecular field analysis (CoMFA), and comparative molecular similarity indices analysis (CoMSIA) of polyhydroxylated N-benzylbenzamide derivatives containing an

Adamantyl N-benzylbenzamide: New series of depigmentation agents with tyrosinase inhibitory activity

Baek, Heung Soo,Hong, Yong Deog,Lee, Chang Seok,Rho, Ho Sik,Shin, Song Seok,Park, Young-Ho,Joo, Yung Hyup

, p. 2110 - 2113 (2012/04/18)

A new series of polyhydroxylated N-benzylbenzamide derivatives containing an adamantyl moiety has been synthesized, and the depigmenting and tyrosinase inhibitory activities of the molecules were evaluated. The lipophilic character of the adamantyl moiety

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