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Propanedioic acid, bis(3-phenyl-2-propynyl)-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16900-65-5 Structure
  • Basic information

    1. Product Name: Propanedioic acid, bis(3-phenyl-2-propynyl)-, diethyl ester
    2. Synonyms:
    3. CAS NO:16900-65-5
    4. Molecular Formula: C25H24O4
    5. Molecular Weight: 388.463
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16900-65-5.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: Propanedioic acid, bis(3-phenyl-2-propynyl)-, diethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Propanedioic acid, bis(3-phenyl-2-propynyl)-, diethyl ester(16900-65-5)
    11. EPA Substance Registry System: Propanedioic acid, bis(3-phenyl-2-propynyl)-, diethyl ester(16900-65-5)
  • 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: 16900-65-5(Hazardous Substances Data)

16900-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16900-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,0 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16900-65:
(7*1)+(6*6)+(5*9)+(4*0)+(3*0)+(2*6)+(1*5)=105
105 % 10 = 5
So 16900-65-5 is a valid CAS Registry Number.

16900-65-5SDS

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 diethyl 2,2-bis(3-phenylprop-2-ynyl)propanedioate

1.2 Other means of identification

Product number -
Other names Bis-(3-phenyl-prop-2-inyl)-malonsaeure-diaethylester

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:16900-65-5 SDS

16900-65-5Relevant articles and documents

Benzannulation through Ruthenium(0)-Catalyzed Transfer Hydrogenative Cycloaddition: Precision Synthesis and Photophysical Characterization of Soluble Diindenoperylenes

Suravarapu, Sankar Rao,Parvathaneni, Sai Prathima,Bender, Jon A.,Roberts, Sean T.,Krische, Michael J.

, p. 7504 - 7510 (2020)

The first application of ruthenium(0)-catalyzed 1,2-dione-diyne [2+2+2] cycloaddition to PAH construction is achieved by the precision synthesis of soluble diindenoperylenes (DIPs), the electronic structures of which were investigated using steady-state a

A convergent formal [4 + 2] cycloaddition of 1,6-diynes and benzyl azides: Construction of spiro-polyheterocycles

Bao, Ming,Lu, Wei,Su, Han,Qiu, Lihua,Xu, Xinfang

supporting information, p. 3258 - 3265 (2018/05/22)

A convergent formal [4 + 2] cycloaddition reaction for the construction of structurally appealing spiro-tetrahydroquinolines has been developed, in which, a one-pot reaction is established for the in situ generation of two reagents, a cyclic alkyne and an

Iridium- and rhodium-catalyzed [2+2+2] cycloadditions of diynes with maleimide: A new synthetic route to highly substituted phthalimides

Alvarez, Leonardo X.,Bessières, Bernard,Einhorn, Jacques

experimental part, p. 1376 - 1380 (2009/04/06)

The [2+2+2] cycloaddition of maleimide with α,ω-diynes in the presence of [IrCl(cod)]2 or [RhCl(cod)]2 and DPPE gives cyclohexadiene derivatives which are readily aromatized with DDQ or MnO 2. This two-step procedure gives

Ir and Rh complex-catalyzed intramolecular alkyne-alkyne couplings with carbon monoxide and isocyanides

Shibata, Takanori,Yamashita, Koji,Katayama, Emi,Takagi, Kentaro

, p. 8661 - 8667 (2007/10/03)

Intramolecular [2+2+1] cycloaddition of diynes with carbon monoxide was catalyzed by Vaska's complex (IrCl(CO)(PPh3)2) or IrCl(cod)(dppp), and cyclopentadienones were obtained in good to high yields. The first catalytic synthesis of

Cyclisation of Acetylenecarboxylic Acid. Synthesis of γ-Methylenebutyrolactones

Yamamato, Makoto

, p. 582 - 587 (2007/10/02)

Various γ-exo-methylenebutyrolactones have been synthesized in excellent yield by the cyclisation of acetylenecarboxylic acids in the presence of a catalytic amount of mercury(II) oxide.Cyclisation of terminal acetylene compounds proceeded regioselectively to give γ-exo-methylenebutyrolactones as the sole product.Disubstituted acetylenes also gave the (Z)-configurational enol lactone, but small amounts of an (E)-isomer of a γ-exo-enol lactone and a δ-lactone (α-pyrone) were also formed.Spectral properties and stereochemistry of the exo-enol lactones are also discussed.

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