Welcome to LookChem.com Sign In|Join Free
  • or
Pyrimidine, 2,4-dimethyl-6-(2-phenylethenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84586-36-7

Post Buying Request

84586-36-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

84586-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84586-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,8 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84586-36:
(7*8)+(6*4)+(5*5)+(4*8)+(3*6)+(2*3)+(1*6)=167
167 % 10 = 7
So 84586-36-7 is a valid CAS Registry Number.

84586-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethyl-4(E)-styrylpyrimidine

1.2 Other means of identification

Product number -
Other names 2,4-Dimethyl-6trans(?)-styryl-pyrimidin

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:84586-36-7 SDS

84586-36-7Relevant academic research and scientific papers

Studies on Pyrimidine Derivatives. XXXVI. Reaction of 6-Substituted 2,4-Dimethylpyrimidines with Benzaldehyde in the Presence of Zinc Chloride

Sakamoto, Takao,Yoshizawa, Hiroshi,Yamanaka, Hiroshi

, p. 2005 - 2010 (2007/10/02)

The condensation of 2,4(2,6)-dimethylpyrimidines (7a-c), but not 6-methoxy-2,4-dimethylpyrimidine (7d), with benzaldehyde in the presence of zinc chloride occurred at the 4(6)-methyl group predominantly.In contrast, the reaction of 7d under the same condi

Studies on Pyrimidine Derivatives. XXX. The Palladium-Catalyzed Cross-Coupling Reaction of Iodopyrimidines with Terminal Olefinic Compounds

Sakamoto, Takao,Arakida, Hiroko,Edo, Kiyoto,Yamanaka, Hiroshi

, p. 3647 - 3656 (2007/10/02)

The influence of triphenylphosphine, used as a ligand, on the palladium-catalyzed cross-coupling reaction of iodopyrimidines with olefins such as ethyl acrylate, acrylonitrile, and styrene was investigated.In general, the addition of triphenylphosphine was concluded to retard the reaction in the pyrimidine series.The effect of triphenylphosphine in the monoazine series is also discussed.Keywords - palladium catalyst; carbon-carbon bond formation; homo-coupling reaction of N-heteroaromatic iodide; raction conditions; six-membered N-heteroaromatic iodide; substituted ethenylpyrimidine

Synthesis of pyrimidine derivatives having olefinic substituents by palladium-catalyzed cross-coupling reaction of iodopyrimidines

Sakamoto, Takao,Arakida, Hiroko,Edo, Kiyoto,Yamanaka, Hiroshi

, p. 965 - 968 (2007/10/02)

The palladium-catalyzed cross-coupling reactions of 2- and 4-iodopyrimidines with olefins were investigated on the stand-point of synthetic chemistry.The reaction was well catalyzed by use of palladium(II) acetate alone, palladium black, or palladium char

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 84586-36-7