Cas 1144038-49-2,p-propargyloxybenzamido-2,3,6,2',3',4',6'-hepta-O-acetyl-β-lactoside

1144038-49-2

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Basic information

Product Name: p-propargyloxybenzamido-2,3,6,2',3',4',6'-hepta-O-acetyl-β-lactoside
Synonyms: p-propargyloxybenzamido-2,3,6,2',3',4',6'-hepta-O-acetyl-β-lactoside
CAS NO:1144038-49-2
Molecular Formula:
Molecular Weight: 793.733
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: p-propargyloxybenzamido-2,3,6,2',3',4',6'-hepta-O-acetyl-β-lactoside(CAS DataBase Reference)
NIST Chemistry Reference: p-propargyloxybenzamido-2,3,6,2',3',4',6'-hepta-O-acetyl-β-lactoside(1144038-49-2)
EPA Substance Registry System: p-propargyloxybenzamido-2,3,6,2',3',4',6'-hepta-O-acetyl-β-lactoside(1144038-49-2)

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: 1144038-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1144038-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,4,0,3 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1144038-49:
(9*1)+(8*1)+(7*4)+(6*4)+(5*0)+(4*3)+(3*8)+(2*4)+(1*9)=122
122 % 10 = 2
So 1144038-49-2 is a valid CAS Registry Number.

1144038-49-2Upstream product

96327-77-4 4-(prop-2-yn-1-yloxy)benzoyl chloride

1144038-49-2Downstream Products

1144038-50-5 p-propargyloxybenzamido-β-lactoside

1144038-49-2Relevant academic research and scientific papers

Regioselective and quantitative modification of cellulose to access cellulose-based advanced materials: Cellulose-based glyeoclusters

Yamashita, Erika,Okubo, Kiyomi,Negishi, Kaori,Hasegawa, Teruaki

, p. 122 - 123 (2009)

Regioselective and quantitative introduction of multiple β-lactoside modules onto the 6C-position of cellulose was achieved through regioselective bromination/azidation of cellulose and the following Cu+-catalyzed chemoselective coupling with a

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