Cas 141367-26-2,2,8,19,25-Tetraazahexacosanedioic acid, 7,20-dioxo-, bis(phenylmethyl) ester

141367-26-2

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Basic information

Product Name: 2,8,19,25-Tetraazahexacosanedioic acid, 7,20-dioxo-, bis(phenylmethyl) ester
Synonyms:
CAS NO:141367-26-2
Molecular Formula: C36H54N4O6
Molecular Weight: 638.848
EINECS: N/A
Product Categories: N/A
Mol File: 141367-26-2.mol
Article Data: 1

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: 2,8,19,25-Tetraazahexacosanedioic acid, 7,20-dioxo-, bis(phenylmethyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,8,19,25-Tetraazahexacosanedioic acid, 7,20-dioxo-, bis(phenylmethyl) ester(141367-26-2)
EPA Substance Registry System: 2,8,19,25-Tetraazahexacosanedioic acid, 7,20-dioxo-, bis(phenylmethyl) ester(141367-26-2)

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: 141367-26-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141367-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,6 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141367-26:
(8*1)+(7*4)+(6*1)+(5*3)+(4*6)+(3*7)+(2*2)+(1*6)=112
112 % 10 = 2
So 141367-26-2 is a valid CAS Registry Number.

141367-26-2Upstream product

141367-26-2Downstream Products

141367-26-2Relevant articles and documents

Further investigation on methoctramine-related tetraamines: Effects of terminal N-substitution and of chain length separating the four nitrogens on M2 muscarinic receptor blocking activity

Minarini,Budriesi,Chiarini,Melchiorre,Tumiatti

, p. 1167 - 1178 (2007/10/02)

A series of tetraamines related to methoctramine (1) was synthesized and evaluated for its blocking activity on M2 and M3 muscarinic receptors of guinea pip left atria and ileum, respectively. Thus, tetraamines 2-7 were synthesized t

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