Cas 1360788-72-2,N4,N4,N9,N9-tetrabenzyl-2,11-dimethyldodeca-5,7-diyne-4,9-diamine

1360788-72-2

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Basic information

Product Name: N₄,N₄,N₉,N₉-tetrabenzyl-2,11-dimethyldodeca-5,7-diyne-4,9-diamine
Synonyms: N₄,N₄,N₉,N₉-tetrabenzyl-2,11-dimethyldodeca-5,7-diyne-4,9-diamine
CAS NO:1360788-72-2
Molecular Formula:
Molecular Weight: 580.857
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: N₄,N₄,N₉,N₉-tetrabenzyl-2,11-dimethyldodeca-5,7-diyne-4,9-diamine(CAS DataBase Reference)
NIST Chemistry Reference: N₄,N₄,N₉,N₉-tetrabenzyl-2,11-dimethyldodeca-5,7-diyne-4,9-diamine(1360788-72-2)
EPA Substance Registry System: N₄,N₄,N₉,N₉-tetrabenzyl-2,11-dimethyldodeca-5,7-diyne-4,9-diamine(1360788-72-2)

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: 1360788-72-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1360788-72-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,7,8 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1360788-72:
(9*1)+(8*3)+(7*6)+(6*0)+(5*7)+(4*8)+(3*8)+(2*7)+(1*2)=182
182 % 10 = 2
So 1360788-72-2 is a valid CAS Registry Number.

1360788-72-2Upstream product

1360788-64-2 N,N-dibenzyl-5-methyl-1-hexyn-3-amine

1360788-72-2Downstream Products

1360788-72-2Relevant academic research and scientific papers

Copper(I)-catalyzed deacetylenative coupling of propargylic amines: An efficient synthesis of symmetric 1,4-diamino-2-butynes

Kim, Yongeun,Nakamura, Hiroyuki

supporting information; scheme or table, p. 12561 - 12563 (2011/12/03)

Deacetylenative coupling: Propargylic amines undergo copper-catalyzed deacetylenative coupling to give the symmetric 1,4-diamino-2-butynes. In the presence of a base, the Glaser-type homocoupling takes place, whereas in the absence of a base the deacetylenative coupling takes place (see scheme).

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