Cas 88719-67-9,Butyl-carbamic acid 4-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-pentyl ester

88719-67-9

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Basic information

Product Name: Butyl-carbamic acid 4-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-pentyl ester
Synonyms: Butyl-carbamic acid 4-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-pentyl ester
CAS NO:88719-67-9
Molecular Formula:
Molecular Weight: 354.447
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: Butyl-carbamic acid 4-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-pentyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Butyl-carbamic acid 4-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-pentyl ester(88719-67-9)
EPA Substance Registry System: Butyl-carbamic acid 4-[2-(3,4-dihydroxy-phenyl)-2-hydroxy-ethylamino]-pentyl ester(88719-67-9)

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: 88719-67-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88719-67-9 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, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88719-67:
(7*8)+(6*8)+(5*7)+(4*1)+(3*9)+(2*6)+(1*7)=189
189 % 10 = 9
So 88719-67-9 is a valid CAS Registry Number.

88719-67-9Upstream product

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88719-67-9Relevant 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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