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103594-72-5

2(1H)-Pyrimidinone, 5-bromo-3,4-dihydro-4-phenyl-1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103594-72-5 Structure

  • Basic information

    1. Product Name: 2(1H)-Pyrimidinone, 5-bromo-3,4-dihydro-4-phenyl-1-(phenylmethyl)-
    2. Synonyms:
    3. CAS NO:103594-72-5
    4. Molecular Formula: C17H15BrN2O
    5. Molecular Weight: 343.223
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103594-72-5.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: 2(1H)-Pyrimidinone, 5-bromo-3,4-dihydro-4-phenyl-1-(phenylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2(1H)-Pyrimidinone, 5-bromo-3,4-dihydro-4-phenyl-1-(phenylmethyl)-(103594-72-5)
    11. EPA Substance Registry System: 2(1H)-Pyrimidinone, 5-bromo-3,4-dihydro-4-phenyl-1-(phenylmethyl)-(103594-72-5)

  • 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: 103594-72-5(Hazardous Substances Data)

103594-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103594-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,9 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103594-72:
(8*1)+(7*0)+(6*3)+(5*5)+(4*9)+(3*4)+(2*7)+(1*2)=115
115 % 10 = 5
So 103594-72-5 is a valid CAS Registry Number.

103594-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-5-bromo-3,4-dihydro-4-phenyl-2(1H)-pyrimidinone

1.2 Other means of identification

Product number -
Other names 1-Benzyl-5-bromo-4-phenyl-3,4-dihydro-1H-pyrimidin-2-one

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:103594-72-5 SDS

103594-72-5Relevant articles and documents

Aryl- and Alkynyltri-isopropoxytitanium Reagents in Regioselective Carbon-Carbon Bond Formation in Azines

Gundersen, Lise-Lotte,Rise, Frode,Undheim, Kjell

, p. 5647 - 5656 (2007/10/02)

Regioselective arylation in the 4-position in pyridines results from 1:1-adduct formation between an aryltriisopropoxytitanium reagent and N-isobutyloxycarbonyl- or an N-silyloxymethyl-3-cyanopyridinium salt after successive DDQ dehydrogenation and cleavage of the 1-substituent.Complete regioselectivity for new C-C bond formation in the 4-position results in the adduct formation between aryl- and phenylethynyltri-isopropoxytitanium reagents and pyrimidin-2(1H)-ones; with ethynyltriisopropoxytitanium the new C-C bond formation occurs at the 6-position.

Structure Investigations on Products from the Reaction of Organocopper, Organolithium and Organomagnesium Reagents with 2(1H)-Pyrimidinones

Rise, Frode,Romming, Christian,Undheim, Kjell

, p. 459 - 468 (2007/10/02)

Alkyl- and arylcuprates and alkyl- and aryllithium and -magnesium reagents form 3,4- or/and 3,6-adducts with 1-benzyl-2(1H)pyrimidinones.The effect of 5-halo substituents on the reactivity and regioselectivity is reported.Structure analyses were made by NMR spectroscopy.Dehydrogenation gives the conjugated, substituted pyrimidinines.X-Ray crystallographic data for 1-benzyl-5-chloro-4-phenyl-2(1H)-pyrimidinone and its regioisomer 1-benzyl-5-chloro-6-phenyl-2(1H)-pyrimidinone are discussed.

Regioselectivity in the Reactions of Aryltri-isopropoxytitanium with Pyrimidinones.

Rise, Frode,Undheim, Kjell

, p. 1997 - 2000 (2007/10/02)

Complete regioselectivity is observed in the 1:1-adduct formation between aryltri-isopropoxytitanium reagents and pyrimidin-2(1H)ones: the new carbon-carbon-bond is formed at C-4.Dehydrogenation gives the arylated, fully conjugated heterocycle.

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