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138924-43-3

trans-3-phenyl-2-propen-1-ol-2-2H is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138924-43-3 Structure

  • Basic information

    1. Product Name: trans-3-phenyl-2-propen-1-ol-2-2H
    2. Synonyms: trans-3-phenyl-2-propen-1-ol-2-2H
    3. CAS NO:138924-43-3
    4. Molecular Formula:
    5. Molecular Weight: 135.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138924-43-3.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: trans-3-phenyl-2-propen-1-ol-2-2H(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-3-phenyl-2-propen-1-ol-2-2H(138924-43-3)
    11. EPA Substance Registry System: trans-3-phenyl-2-propen-1-ol-2-2H(138924-43-3)

  • 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: 138924-43-3(Hazardous Substances Data)

138924-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138924-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,2 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138924-43:
(8*1)+(7*3)+(6*8)+(5*9)+(4*2)+(3*4)+(2*4)+(1*3)=153
153 % 10 = 3
So 138924-43-3 is a valid CAS Registry Number.

138924-43-3Upstream product

138924-43-3Relevant articles and documents

Mechanistic Insight into the Dehydro-Diels-Alder Reaction of Styrene-Ynes

Kocsis, Laura S.,Kagalwala, Husain N.,Mutto, Sharlene,Godugu, Bhaskar,Bernhard, Stefan,Tantillo, Dean J.,Brummond, Kay M.

, p. 11686 - 11698 (2015)

The Diels-Alder reaction represents one of the most thoroughly studied and well-understood synthetic transformations for the assembly of six-membered rings. Although intramolecular dehydro-Diels-Alder (IMDDA) reactions have previously been employed for th

Hydroamination versus Allylic Amination in Iridium-Catalyzed Reactions of Allylic Acetates with Amines: 1,3-Aminoalcohols via Ester-Directed Regioselectivity

Kim, Seung Wook,Wurm, Thomas,Brito, Gilmar A.,Jung, Woo-Ok,Zbieg, Jason R.,Stivala, Craig E.,Krische, Michael J.

supporting information, p. 9087 - 9090 (2018/08/03)

In the presence of a neutral dppf-modified iridium catalyst and Cs2CO3, linear allylic acetates react with primary amines to form products of hydroamination with complete 1,3-regioselectivity. The collective data, including deuterium labeling studies, corroborate a catalytic mechanism involving rapid, reversible acetate-directed aminoiridation with inner-sphere/outer-sphere crossover followed by turnover-limiting proto-demetalation mediated by amine.

Asymmetric catalysis. Mechanism of asymmetric catalytic intramolecular hydrosilation

Bergens, Steven H.,Noheda, Pedro,Whelan, John,Bosnich

, p. 2128 - 2135 (2007/10/02)

The mechanism of asymmetric catalytic intramolecular hydrosilation using [Rh(diphosphine)]+ catalysts has been investigated by the use of specifically labeled deuterated substrates. It is concluded that oxidative addition of the silicon hydride

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