Cas 884324-38-3,6,6,8,8-tetraisopropyl-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-10<i>H</i>-5,7,9-trioxa-6,8-disila-benzocyclooctene

884324-38-3

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Basic information

Product Name: 6,6,8,8-tetraisopropyl-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-10H-5,7,9-trioxa-6,8-disila-benzocyclooctene
Synonyms: 6,6,8,8-tetraisopropyl-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-10H-5,7,9-trioxa-6,8-disila-benzocyclooctene
CAS NO:884324-38-3
Molecular Formula:
Molecular Weight: 669.021
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: 6,6,8,8-tetraisopropyl-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-10H-5,7,9-trioxa-6,8-disila-benzocyclooctene(CAS DataBase Reference)
NIST Chemistry Reference: 6,6,8,8-tetraisopropyl-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-10H-5,7,9-trioxa-6,8-disila-benzocyclooctene(884324-38-3)
EPA Substance Registry System: 6,6,8,8-tetraisopropyl-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-10H-5,7,9-trioxa-6,8-disila-benzocyclooctene(884324-38-3)

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: 884324-38-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 884324-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,3,2 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 884324-38:
(8*8)+(7*8)+(6*4)+(5*3)+(4*2)+(3*4)+(2*3)+(1*8)=193
193 % 10 = 3
So 884324-38-3 is a valid CAS Registry Number.

884324-38-3Upstream product

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884324-38-3Relevant academic research and scientific papers

A novel linker for solid-phase synthesis cleavable under neutral conditions

Murata, Asako,Wada, Takeshi

, p. 2147 - 2150 (2006)

A novel linker cleavable under neutral conditions has been developed for the solid-phase synthesis of base-labile compounds. The linker is comprised of a 3-azidomethyl-4-hydroxybenzyl alcohol moiety, and the azidomethyl group in the linker is readily conv

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