Cas 413615-81-3,Cyclopropa[cd]pentalene-1-methanol, 1,2,2a,2b,4a,4b-hexahydro-4b-hydroxy- (9CI)

413615-81-3

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Basic information

Product Name: Cyclopropa[cd]pentalene-1-methanol, 1,2,2a,2b,4a,4b-hexahydro-4b-hydroxy- (9CI)
Synonyms: Cyclopropa[cd]pentalene-1-methanol, 1,2,2a,2b,4a,4b-hexahydro-4b-hydroxy- (9CI)
CAS NO:413615-81-3
Molecular Formula: C9H12O2
Molecular Weight: 152.19038
EINECS: N/A
Product Categories: CYCLOPENTANE
Mol File: 413615-81-3.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Cyclopropa[cd]pentalene-1-methanol, 1,2,2a,2b,4a,4b-hexahydro-4b-hydroxy- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Cyclopropa[cd]pentalene-1-methanol, 1,2,2a,2b,4a,4b-hexahydro-4b-hydroxy- (9CI)(413615-81-3)
EPA Substance Registry System: Cyclopropa[cd]pentalene-1-methanol, 1,2,2a,2b,4a,4b-hexahydro-4b-hydroxy- (9CI)(413615-81-3)

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: 413615-81-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 413615-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,3,6,1 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 413615-81:
(8*4)+(7*1)+(6*3)+(5*6)+(4*1)+(3*5)+(2*8)+(1*1)=123
123 % 10 = 3
So 413615-81-3 is a valid CAS Registry Number.

413615-81-3Upstream product

413615-81-3Downstream Products

413615-81-3Relevant academic research and scientific papers

Synthesis of 2-silaoxane via 1,3- photocycloaddition

Bahu, Suhail,Fleming, Steven A.,Nilsson, Brad,Turner, Tim

, p. 1341 - 1344 (2001)

Irradiation of an aryl group with a silyl tethered alkene yields a tetracyclic 2-silaoxane with high regioselectivity. The multicyclic structure has been further modified to give an unstable tricyclic diol. Photocycloaddition between cyclopentene and phen

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