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76936-19-1

Phosphorane, (1,5-dimethyl-4-hexenylidene)triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76936-19-1 Structure

  • Basic information

    1. Product Name: Phosphorane, (1,5-dimethyl-4-hexenylidene)triphenyl-
    2. Synonyms:
    3. CAS NO:76936-19-1
    4. Molecular Formula: C26H29P
    5. Molecular Weight: 372.49
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76936-19-1.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: Phosphorane, (1,5-dimethyl-4-hexenylidene)triphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphorane, (1,5-dimethyl-4-hexenylidene)triphenyl-(76936-19-1)
    11. EPA Substance Registry System: Phosphorane, (1,5-dimethyl-4-hexenylidene)triphenyl-(76936-19-1)

  • 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: 76936-19-1(Hazardous Substances Data)

76936-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76936-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,3 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76936-19:
(7*7)+(6*6)+(5*9)+(4*3)+(3*6)+(2*1)+(1*9)=171
171 % 10 = 1
So 76936-19-1 is a valid CAS Registry Number.

76936-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1,5-Dimethyl-4-hexenylidene)-triphenylphosphorane

1.2 Other means of identification

Product number -
Other names -

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:76936-19-1 SDS

76936-19-1Relevant articles and documents

Towards the enantioselective synthesis of anti-HIV agents litseaverticillols C and K from d-glucose

Mohapatra, Debendra K.,Mondal, Dhananjoy,Gurjar, Mukund K.

, p. 2613 - 2621 (2007/10/03)

The first enantioselective synthesis towards the litseaverticillols C and K has been achieved, from d-glucose, using the ring closing metathesis (RCM) and Wittig reactions as key steps.

Biosynthesis of (+)-epicubenol

Cane, David E.,Tandon, Manish

, p. 5355 - 5358 (2007/10/02)

Incubation of [6-2H]FPP (14a) with epicubenol synthase isolated from Streptomyces sp. LL-B7 gave epicubenol (1c) labeled at D-9 as established by 2H NMR. These results confirm the involvement of a predicted 1,2-hydride shift in the mechanism of formation of 1.

SYNTHESIS OF (+/-)-PREPINNATERPENE, A BROMODITERPENE FROM THE RED ALGA LAURENCIA PINNATA YAMADA

Fukuzawa, Akio,Sato, Hideaki,Masamune, Tadashi

, p. 4303 - 4306 (2007/10/02)

A total synthesis of (+/-)-prepinnaterpene, a brominated diterpene with a unique skeleton, and (+/-)-oppositol, a related sesquiterpene, is described.

166. Synthesis of the Sesquirose Oxides from Rose Oxide

Ohloff, Guenther,Giersch, Wolfgang,Decorzant, Rene,Buechi, George

, p. 1589 - 1597 (2007/10/02)

The eight stereoisomeric sesquirose oxides 9 to 16 were prepared from the four optically active rose oxides 1 to 4.The spectral data, optical rotations and the olfactive properties of 9 to 16 are given.

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