Basic information

Product Name: Phosphonium, (1-ethoxyethyl)triphenyl-, bromide
Synonyms:
CAS NO:95209-71-5
Molecular Formula: C22H24OP.Br
Molecular Weight: 415.31
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: Phosphonium, (1-ethoxyethyl)triphenyl-, bromide(CAS DataBase Reference)
NIST Chemistry Reference: Phosphonium, (1-ethoxyethyl)triphenyl-, bromide(95209-71-5)
EPA Substance Registry System: Phosphonium, (1-ethoxyethyl)triphenyl-, bromide(95209-71-5)

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: 95209-71-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95209-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,0 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95209-71:
(7*9)+(6*5)+(5*2)+(4*0)+(3*9)+(2*7)+(1*1)=145
145 % 10 = 5
So 95209-71-5 is a valid CAS Registry Number.

95209-71-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-ethoxyethyl(triphenyl)phosphanium,bromide

1.2 Other means of identification

Product number	-
Other names	Phosphonium,(1-ethoxyethyl)triphenyl-,bromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:95209-71-5 SDS

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95209-71-5Relevant academic research and scientific papers

ENOL ETHERS : PREPARATION AND SYNTHETIC APPLICATIONS

Ousset, J. B.,Mioskowski, C.,Yang, Y.-L.,Falck, J. R.

, p. 5903 - 5906 (2007/10/02)

A versatile preparation of α-alkoxyphosphonium bromides leading to enol ethers by Wittig coupling was exploited for the convergent synthesis of pheromones from the Douglas-fir tussock moth and the olive fly Dacus oleae as well as an oxaspirolactone and C-

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