Cas 74694-14-7,Dimethyl-dithiocarbamic acid (E)-(R)-3-((R)-hydroxy-phenyl-methyl)-4-methyl-pent-1-enyl ester

74694-14-7

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Basic information

Product Name: Dimethyl-dithiocarbamic acid (E)-(R)-3-((R)-hydroxy-phenyl-methyl)-4-methyl-pent-1-enyl ester
Synonyms:
CAS NO:74694-14-7
Molecular Formula:
Molecular Weight: 309.497
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: Dimethyl-dithiocarbamic acid (E)-(R)-3-((R)-hydroxy-phenyl-methyl)-4-methyl-pent-1-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Dimethyl-dithiocarbamic acid (E)-(R)-3-((R)-hydroxy-phenyl-methyl)-4-methyl-pent-1-enyl ester(74694-14-7)
EPA Substance Registry System: Dimethyl-dithiocarbamic acid (E)-(R)-3-((R)-hydroxy-phenyl-methyl)-4-methyl-pent-1-enyl ester(74694-14-7)

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: 74694-14-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 74694-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,9 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74694-14:
(7*7)+(6*4)+(5*6)+(4*9)+(3*4)+(2*1)+(1*4)=157
157 % 10 = 7
So 74694-14-7 is a valid CAS Registry Number.

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74694-14-7Relevant academic research and scientific papers

DIASTEREOSELECTION IN THE REACTIONS OF THIOALLYLIC ANIONS WITH BENZALDEHYDE

Hayashi, Toshio,Fujitaka, Nobuo,Oishi, Takeshi,Takeshima, Tatsuo

, p. 303 - 306 (2007/10/02)

Reactions of the anions of (Z)-2-alkenyl N,N-dimethyldithiocarbamates with benzaldehyde gave the erythro isomers of 4-hydroxy-4-phenyl-(E)-1-alkenyl N,N-dimethyldithiocarbamates stereoselectively, and those of the anions of (E)-2-alkenyl N,N-dimethyldithiocarbamates afforded the threo isomers predominantly.

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