Cas 136603-08-2,1-phenylseleno-5,13-dioxa-6,14-dioxo-7,15-dimethylene-17-cyano-17-methyl octadecane

136603-08-2

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Basic information

Product Name: 1-phenylseleno-5,13-dioxa-6,14-dioxo-7,15-dimethylene-17-cyano-17-methyl octadecane
Synonyms:
CAS NO:136603-08-2
Molecular Formula:
Molecular Weight: 504.528
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: 1-phenylseleno-5,13-dioxa-6,14-dioxo-7,15-dimethylene-17-cyano-17-methyl octadecane(CAS DataBase Reference)
NIST Chemistry Reference: 1-phenylseleno-5,13-dioxa-6,14-dioxo-7,15-dimethylene-17-cyano-17-methyl octadecane(136603-08-2)
EPA Substance Registry System: 1-phenylseleno-5,13-dioxa-6,14-dioxo-7,15-dimethylene-17-cyano-17-methyl octadecane(136603-08-2)

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: 136603-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136603-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,6,0 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 136603-08:
(8*1)+(7*3)+(6*6)+(5*6)+(4*0)+(3*3)+(2*0)+(1*8)=112
112 % 10 = 2
So 136603-08-2 is a valid CAS Registry Number.

136603-08-2Upstream product

132841-90-8 ω-phenylseleno((CH2)4)-2-(tri-n-butylstannylmethyl)propenoate ester

136603-08-2Downstream Products

136603-08-2Relevant academic research and scientific papers

Intramolecular SH2 macrocyclisations

Baldwin, Jack E.,Adlington, Robert M.,Mitchell, Mark B.,Robertson, Jeremy

, p. 5901 - 5918 (2007/10/02)

The synthesis of 10-15 membered α-methylene macrocyclic lactones from the functionalised allylstannanes (7e)-(7j) is described. Attempts to synthesise analogous 6-9 membered lactones proved unsuccessful, resulting instead in the production of dilactones and AIBN derived adducts.

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