Cas 183273-10-1,{4-[4-Bromo-3-(9H-fluoren-9-ylmethoxycarbonylamino)-phenoxymethyl]-phenoxy}-acetic acid allyl ester

183273-10-1

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Basic information

Product Name: {4-[4-Bromo-3-(9H-fluoren-9-ylmethoxycarbonylamino)-phenoxymethyl]-phenoxy}-acetic acid allyl ester
Synonyms: {4-[4-Bromo-3-(9H-fluoren-9-ylmethoxycarbonylamino)-phenoxymethyl]-phenoxy}-acetic acid allyl ester
CAS NO:183273-10-1
Molecular Formula:
Molecular Weight: 614.492
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: {4-[4-Bromo-3-(9H-fluoren-9-ylmethoxycarbonylamino)-phenoxymethyl]-phenoxy}-acetic acid allyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {4-[4-Bromo-3-(9H-fluoren-9-ylmethoxycarbonylamino)-phenoxymethyl]-phenoxy}-acetic acid allyl ester(183273-10-1)
EPA Substance Registry System: {4-[4-Bromo-3-(9H-fluoren-9-ylmethoxycarbonylamino)-phenoxymethyl]-phenoxy}-acetic acid allyl ester(183273-10-1)

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: 183273-10-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183273-10-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,2,7 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 183273-10:
(8*1)+(7*8)+(6*3)+(5*2)+(4*7)+(3*3)+(2*1)+(1*0)=131
131 % 10 = 1
So 183273-10-1 is a valid CAS Registry Number.

183273-10-1Upstream product

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183273-10-1Relevant academic research and scientific papers

Heck reaction on solid support: Synthesis of indole analogs

Yun, Weiya,Mohan, Raju

, p. 7189 - 7192 (1996)

The intramolecular Heck reaction of polymer bound arylhalides such as 1 affords indole analogs 11 in high yield. The precursor is readily assembled from acid chlorides and allylic bromides and offers an approach to diverse libraries of indole analogs.

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