Cas 1610016-14-2,dimethyl 3,3-[(2,5-dimethyl-1,4-phenylene)bis(methylenethio)]dipropanoate

1610016-14-2

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Basic information

Product Name: dimethyl 3,3-[(2,5-dimethyl-1,4-phenylene)bis(methylenethio)]dipropanoate
Synonyms: dimethyl 3,3-[(2,5-dimethyl-1,4-phenylene)bis(methylenethio)]dipropanoate
CAS NO:1610016-14-2
Molecular Formula:
Molecular Weight: 370.534
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 3,3-[(2,5-dimethyl-1,4-phenylene)bis(methylenethio)]dipropanoate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl 3,3-[(2,5-dimethyl-1,4-phenylene)bis(methylenethio)]dipropanoate(1610016-14-2)
EPA Substance Registry System: dimethyl 3,3-[(2,5-dimethyl-1,4-phenylene)bis(methylenethio)]dipropanoate(1610016-14-2)

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: 1610016-14-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1610016-14-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,0,1 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1610016-14:
(9*1)+(8*6)+(7*1)+(6*0)+(5*0)+(4*1)+(3*6)+(2*1)+(1*4)=92
92 % 10 = 2
So 1610016-14-2 is a valid CAS Registry Number.

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1610016-14-2Relevant academic research and scientific papers

Stereoselective synthesis of dithia[3.3]cyclophane S,S'-dioxides with planar and central chirality

Barattucci, Anna,Di Gioia, Maria Luisa,Leggio, Antonella,Minuti, Lucio,Papalia, Teresa,Siciliano, Carlo,Temperini, Andrea,Bonaccorsi, Paola

, p. 2099 - 2104 (2014)

5,8-Dimethyl-1,12-dimethylene-2,11-dithia[3.3]cyclophane 2,11-dioxides with planar and central chirality were synthesized in high yields, starting from 2,5-dimethyl-1,4-benzenedimethanethiol, through the formation of suitable transient sulfenic functions

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