Cas 1383577-45-4,9,22-dioxa-1,12,13,14,25,26-hexaazapentacyclo[22.2.1.111,14.02,7.015,20]octacosa-2,4,6,11(28),12,15,17,19,24(27),25-decaene-8,21-dione

1383577-45-4

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Basic information

Product Name: 9,22-dioxa-1,12,13,14,25,26-hexaazapentacyclo[22.2.1.1^11,14.0^2,7.0^15,20]octacosa-2,4,6,11⁽²⁸⁾,12,15,17,19,24⁽²⁷⁾,25-decaene-8,21-dione
Synonyms: 9,22-dioxa-1,12,13,14,25,26-hexaazapentacyclo[22.2.1.1^11,14.0^2,7.0^15,20]octacosa-2,4,6,11⁽²⁸⁾,12,15,17,19,24⁽²⁷⁾,25-decaene-8,21-dione
CAS NO:1383577-45-4
Molecular Formula:
Molecular Weight: 402.369
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: 9,22-dioxa-1,12,13,14,25,26-hexaazapentacyclo[22.2.1.1^11,14.0^2,7.0^15,20]octacosa-2,4,6,11⁽²⁸⁾,12,15,17,19,24⁽²⁷⁾,25-decaene-8,21-dione(CAS DataBase Reference)
NIST Chemistry Reference: 9,22-dioxa-1,12,13,14,25,26-hexaazapentacyclo[22.2.1.1^11,14.0^2,7.0^15,20]octacosa-2,4,6,11⁽²⁸⁾,12,15,17,19,24⁽²⁷⁾,25-decaene-8,21-dione(1383577-45-4)
EPA Substance Registry System: 9,22-dioxa-1,12,13,14,25,26-hexaazapentacyclo[22.2.1.1^11,14.0^2,7.0^15,20]octacosa-2,4,6,11⁽²⁸⁾,12,15,17,19,24⁽²⁷⁾,25-decaene-8,21-dione(1383577-45-4)

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: 1383577-45-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1383577-45-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,5,7 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1383577-45:
(9*1)+(8*3)+(7*8)+(6*3)+(5*5)+(4*7)+(3*7)+(2*4)+(1*5)=194
194 % 10 = 4
So 1383577-45-4 is a valid CAS Registry Number.

1383577-45-4Upstream product

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1383577-45-4Relevant academic research and scientific papers

Study of direct macrocycle formation via the cyclisation of propargyl 2-azidobenzoate

Hradilová, Ludmila,Grepl, Martin,Dvo?áková, Barbora,Hradil, Pavel

, p. 1218 - 1221 (2013)

Macrocycles were synthesised via the cyclisation of propargyl 2-azidobenzoate using 'click' chemistry. An LC/MS-based method for the separation of macrocycles is described. In the present work, the influence of various catalysts and reaction conditions on

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