Cas 1415638-79-7,N-(1-phenyl-5-(p-tolyl)penta-2,4-diyn-1-yl)-4-methylbenzenesulfonamide

1415638-79-7

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Basic information

Product Name: N-(1-phenyl-5-(p-tolyl)penta-2,4-diyn-1-yl)-4-methylbenzenesulfonamide
Synonyms: N-(1-phenyl-5-(p-tolyl)penta-2,4-diyn-1-yl)-4-methylbenzenesulfonamide
CAS NO:1415638-79-7
Molecular Formula:
Molecular Weight: 399.513
EINECS: N/A
Product Categories: N/A
Mol File: 1415638-79-7.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: N-(1-phenyl-5-(p-tolyl)penta-2,4-diyn-1-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(1-phenyl-5-(p-tolyl)penta-2,4-diyn-1-yl)-4-methylbenzenesulfonamide(1415638-79-7)
EPA Substance Registry System: N-(1-phenyl-5-(p-tolyl)penta-2,4-diyn-1-yl)-4-methylbenzenesulfonamide(1415638-79-7)

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: 1415638-79-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415638-79-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,6,3 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1415638-79:
(9*1)+(8*4)+(7*1)+(6*5)+(5*6)+(4*3)+(3*8)+(2*7)+(1*9)=167
167 % 10 = 7
So 1415638-79-7 is a valid CAS Registry Number.

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1415638-79-7Relevant articles and documents

Catalytic enantioselective addition of terminal 1,3-diynes to N-sulfonyl aldimines: Access to chiral diynylated carbinamines

Liu, Tian-Lin,Zhang, Heng-Xia,Zheng, Yan,Yao, Qingwei,Ma, Jun-An

supporting information, p. 12234 - 12236 (2013/01/16)

An efficient method for the asymmetric synthesis of chiral diynylated carbinamines is described. The direct catalytic enantioselective addition of terminal 1,3-diynes to N-sulfonyl aldimines proceeded smoothly under mild reaction conditions to produce diy

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