Cas 253441-69-9,2-[(4-biphenyl)oxymethyl]-4-(4-oxo-3,4-dihydro-1,2,3-benzotriazin-3-yl)butyric acid

253441-69-9

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Basic information

Product Name: 2-[(4-biphenyl)oxymethyl]-4-(4-oxo-3,4-dihydro-1,2,3-benzotriazin-3-yl)butyric acid
Synonyms:
CAS NO:253441-69-9
Molecular Formula:
Molecular Weight: 415.448
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: 2-[(4-biphenyl)oxymethyl]-4-(4-oxo-3,4-dihydro-1,2,3-benzotriazin-3-yl)butyric acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(4-biphenyl)oxymethyl]-4-(4-oxo-3,4-dihydro-1,2,3-benzotriazin-3-yl)butyric acid(253441-69-9)
EPA Substance Registry System: 2-[(4-biphenyl)oxymethyl]-4-(4-oxo-3,4-dihydro-1,2,3-benzotriazin-3-yl)butyric acid(253441-69-9)

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: 253441-69-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 253441-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,4,4 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 253441-69:
(8*2)+(7*5)+(6*3)+(5*4)+(4*4)+(3*1)+(2*6)+(1*9)=129
129 % 10 = 9
So 253441-69-9 is a valid CAS Registry Number.

253441-69-9Upstream product

336107-56-3 3-[3-(biphenyl-4-yloxymethyl)-pent-4-enyl]-3H-benzo[d][1,2,3]triazin-4-one

253441-69-9Downstream Products

253441-69-9Relevant academic research and scientific papers

General synthesis of α-substituted 3-bisaryloxy propionic acid derivatives as specific MMP inhibitors

Chollet, Anne-Marie,Le Diguarher, Thierry,Murray, Lynne,Bertrand, Marc,Tucker, Gordon C.,Sabatini, Massimo,Pierre, Alain,Atassi, Ghanem,Bonnet, Jacqueline,Casara, Patrick

, p. 295 - 299 (2007/10/03)

Modulations of α and aryl substitutions on 3-aryloxy propionic acid hydroxamates led to novel and potent inhibitors of MMP-2,3,9 and 13, and selectivity versus MMP-1.

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