Cas 650616-80-1,1,12-bis[7-hydroxymethyl-5,8-dimethoxy-1,4-dihydro-1,4-methanonaphthalen-6-yl]-2,5,8,11-tetraoxadodecane

650616-80-1

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Basic information

Product Name: 1,12-bis[7-hydroxymethyl-5,8-dimethoxy-1,4-dihydro-1,4-methanonaphthalen-6-yl]-2,5,8,11-tetraoxadodecane
Synonyms: 1,12-bis[7-hydroxymethyl-5,8-dimethoxy-1,4-dihydro-1,4-methanonaphthalen-6-yl]-2,5,8,11-tetraoxadodecane
CAS NO:650616-80-1
Molecular Formula:
Molecular Weight: 638.755
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: 1,12-bis[7-hydroxymethyl-5,8-dimethoxy-1,4-dihydro-1,4-methanonaphthalen-6-yl]-2,5,8,11-tetraoxadodecane(CAS DataBase Reference)
NIST Chemistry Reference: 1,12-bis[7-hydroxymethyl-5,8-dimethoxy-1,4-dihydro-1,4-methanonaphthalen-6-yl]-2,5,8,11-tetraoxadodecane(650616-80-1)
EPA Substance Registry System: 1,12-bis[7-hydroxymethyl-5,8-dimethoxy-1,4-dihydro-1,4-methanonaphthalen-6-yl]-2,5,8,11-tetraoxadodecane(650616-80-1)

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: 650616-80-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 650616-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,0,6,1 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 650616-80:
(8*6)+(7*5)+(6*0)+(5*6)+(4*1)+(3*6)+(2*8)+(1*0)=151
151 % 10 = 1
So 650616-80-1 is a valid CAS Registry Number.

650616-80-1Upstream product

19249-03-7 triethylene glycol di-(p-toluenesulfonate)

650616-80-1Downstream Products

650616-80-1Relevant academic research and scientific papers

Periphery-modified crown ethers. Synthesis of bis-5,8-dimethoxy-1,4- methanonaphthalene-fused crown ethers

Chou, Teh-Chang,Chen, Shing-Yi,Chen, Yie-Hsung

, p. 9939 - 9950 (2003)

The easily accessible and multi-functionalized 5,8-dimethoxy-6,7-dihydroxy methyl-1,4-dihydro-1,4-methanonaphthalene (1) has been utilized as the basic building material to synthesize the symmetric bis-methanonaphthalene-fused crown ethers 14a-d (BMN-16-crown-4, BMN-22-crown-6, BMN-28-crown-8, and BMN-34-crown-10), that are constructed based on the connection between the α,β-bis-benzylic carbon atoms of diol 1 and oligoethylene glycols (9a-d) via two synthetic routes keyed upon the method of Williamson ether synthesis.

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