Cas 684236-36-0,bis(2-(bis(4-methoxybenzenesulfonyl)amino)ethyl)-(2-(4-methoxybenzenesulfonamido)ethyl)amine

684236-36-0

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Basic information

Product Name: bis(2-(bis(4-methoxybenzenesulfonyl)amino)ethyl)-(2-(4-methoxybenzenesulfonamido)ethyl)amine
Synonyms: bis(2-(bis(4-methoxybenzenesulfonyl)amino)ethyl)-(2-(4-methoxybenzenesulfonamido)ethyl)amine
CAS NO:684236-36-0
Molecular Formula:
Molecular Weight: 997.18
EINECS: N/A
Product Categories: N/A
Mol File: 684236-36-0.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: bis(2-(bis(4-methoxybenzenesulfonyl)amino)ethyl)-(2-(4-methoxybenzenesulfonamido)ethyl)amine(CAS DataBase Reference)
NIST Chemistry Reference: bis(2-(bis(4-methoxybenzenesulfonyl)amino)ethyl)-(2-(4-methoxybenzenesulfonamido)ethyl)amine(684236-36-0)
EPA Substance Registry System: bis(2-(bis(4-methoxybenzenesulfonyl)amino)ethyl)-(2-(4-methoxybenzenesulfonamido)ethyl)amine(684236-36-0)

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: 684236-36-0(Hazardous Substances Data)

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684236-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 684236-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,4,2,3 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 684236-36:
(8*6)+(7*8)+(6*4)+(5*2)+(4*3)+(3*6)+(2*3)+(1*6)=180
180 % 10 = 0
So 684236-36-0 is a valid CAS Registry Number.

684236-36-0Upstream product

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684236-36-0Relevant articles and documents

Controllable, selective per-functionalization of dendritic oligoamines

Voegtle, Fritz,Fakhrnabavi, Hassan,Lukin, Oleg

, p. 1075 - 1078 (2007/10/03)

A method allowing for an unprecedented controllable functionalization of oligoamines via N,N-bis-sulfonylation with various sulfonyl chlorides has been developed. Depending on the nature of the sufonyl chloride and reaction conditions such as base, time o

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