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21851-76-3

Phosphonium, (2,3-dihydro-1H-inden-1-yl)triphenyl-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21851-76-3 Structure

  • Basic information

    1. Product Name: Phosphonium, (2,3-dihydro-1H-inden-1-yl)triphenyl-, bromide
    2. Synonyms:
    3. CAS NO:21851-76-3
    4. Molecular Formula: C27H24P.Br
    5. Molecular Weight: 459.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21851-76-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Phosphonium, (2,3-dihydro-1H-inden-1-yl)triphenyl-, bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphonium, (2,3-dihydro-1H-inden-1-yl)triphenyl-, bromide(21851-76-3)
    11. EPA Substance Registry System: Phosphonium, (2,3-dihydro-1H-inden-1-yl)triphenyl-, bromide(21851-76-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 21851-76-3(Hazardous Substances Data)

21851-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21851-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,5 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21851-76:
(7*2)+(6*1)+(5*8)+(4*5)+(3*1)+(2*7)+(1*6)=103
103 % 10 = 3
So 21851-76-3 is a valid CAS Registry Number.

21851-76-3SDS

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 2,3-dihydro-1H-inden-1-yl(triphenyl)phosphanium,bromide

1.2 Other means of identification

Product number -
Other names 1-indanyltriphenylphosphonium 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:21851-76-3 SDS

21851-76-3Relevant articles and documents

Novel reaction course of alkenes to phosphonium salts

Okuma, Kentaro,Izaki, Toshiharu

, p. 1831 - 1833 (2005)

The reaction of styrenes with triphenylphosphine in the presence of acid gave the corresponding 1-arylethylphosphonium salts in 76-82% yields. Indene also reacted with triphenylphosphine and tetrafluoroboric acid to afford 1-indanyltriphenylphosphonium te

Rhodium-catalyzed synthesis of 2,3-disubstituted indoles from β,β-Disubstituted stryryl azides

Sun, Ke,Liu, Sheng,Bec, Patryk M.,Driver, Tom G.

, p. 1702 - 1706 (2011/04/24)

Rings la carte: Rhodium carboxylate complexes catalyze selective cascade reactions to produce a range 2,3-disubstituted indoles from β,β- disubstituted stryryl azides. The selective migration of aryl groups appears to originate from a putative phenonium ion reactive intermediate (see scheme).

Synthesis and evaluation of (pyridylmethylene)tetrahydronaphthalenes/- indanes and structurally modified derivatives: Potent and selective inhibitors of aldosterone synthase

Ulmschneider, Sarah,Müller-Vieira, Ursula,Klein, Christian D.,Antes, Iris,Lengauer, Thomas,Hartmann, Rolf W.

, p. 1563 - 1575 (2007/10/03)

Elevated aldosterone levels are key effectors for the development and progression of congestive heart failure and myocardial fibrosis. Recently, we proposed inhibition of aldosterone synthase (CYP11B2) as an innovative strategy for the treatment of these

Synthesis and evaluation of imidazolylmethylenetetrahydronaphthalenes and imidazolylmethyleneindanes: Potent inhibitors of aldosterone synthase

Ulmschneider, Sarah,Müller-Vieira, Ursula,Mitrenga, Markus,Hartmann, Rolf W.,Oberwinkler-Marchais, Sandrine,Klein, Christian D.,Bureik, Matthias,Bernhardt, Rita,Antes, Iris,Lengauer, Thomas

, p. 1796 - 1805 (2007/10/03)

Elevated plasma aldosterone levels play a detrimental role in certain forms of congestive heart failure and myocardial fibrosis. We proposed aldosterone synthase (CYP11B2) as a novel target for the treatment of these diseases. In this study, the synthesis

A SYNTHESIS OF 2-METHYLENEINDANE

McCullough, Kevin J.

, p. 2223 - 2224 (2007/10/02)

After difficulties encountered in a conventional Wittig approach, a synthesis of 2-methyleneindane was achieved via a β-silylsulphone intermediate.

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