Cas 352463-60-6,acetic acid 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxymethyl)-benzyl ester

352463-60-6

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Basic information

Product Name: acetic acid 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxymethyl)-benzyl ester
Synonyms: acetic acid 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxymethyl)-benzyl ester
CAS NO:352463-60-6
Molecular Formula:
Molecular Weight: 325.321
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: acetic acid 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxymethyl)-benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: acetic acid 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxymethyl)-benzyl ester(352463-60-6)
EPA Substance Registry System: acetic acid 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxymethyl)-benzyl ester(352463-60-6)

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: 352463-60-6(Hazardous Substances Data)

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352463-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 352463-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,4,6 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 352463-60:
(8*3)+(7*5)+(6*2)+(5*4)+(4*6)+(3*3)+(2*6)+(1*0)=136
136 % 10 = 6
So 352463-60-6 is a valid CAS Registry Number.

352463-60-6Upstream product

352463-60-6Downstream Products

352463-61-7 acetic acid 4-aminooxymethyl-benzyl ester

352463-60-6Relevant academic research and scientific papers

Solid-phase tandem radical addition-cyclisation reaction of oxime ethers

Miyabe,Fujii,Tanaka,Naito

, p. 831 - 832 (2001)

The solid-phase tandem C-C bond-forming reactions of oxime ethers connected with α,β-unsaturated carbonyl groups proceeded effectively under iodine atom-transfer reaction conditions to give the azacycles or chiral oxacycles after cleavage of the resin.

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