Cas 88719-52-2,p-Tolyl-carbamic acid 5-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-hexyl ester

88719-52-2

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Basic information

Product Name: p-Tolyl-carbamic acid 5-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-hexyl ester
Synonyms: p-Tolyl-carbamic acid 5-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-hexyl ester
CAS NO:88719-52-2
Molecular Formula:
Molecular Weight: 402.491
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: p-Tolyl-carbamic acid 5-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-hexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: p-Tolyl-carbamic acid 5-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-hexyl ester(88719-52-2)
EPA Substance Registry System: p-Tolyl-carbamic acid 5-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-hexyl ester(88719-52-2)

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: 88719-52-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88719-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,1 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88719-52:
(7*8)+(6*8)+(5*7)+(4*1)+(3*9)+(2*5)+(1*2)=182
182 % 10 = 2
So 88719-52-2 is a valid CAS Registry Number.

88719-52-2Upstream product

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88719-52-2Relevant academic research and scientific papers

Conjugates of Catecholamines. 6. Synthesis and β-Adrenergic Activity of N-(Hydroxyalkyl)catecholamine Derivatives

Reitz, Allen B.,Avery, Mitchell A.,Rosenkranz, Roberto P.,Verlander, Michael S.,Melmon, Kenneth L.,et al.

, p. 642 - 647 (2007/10/02)

A new series of catecholamines has been prepared in which the N-alkyl substituent of dl-epinephrine or dl-isoproterenol has been extended by a methylene chain terminated by a hydroxyl group or derived functionality (e.g., carbamate or ester).These functio

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