Welcome to LookChem.com Sign In|Join Free
  • or
Phenol, 2,6-bis(1,1-dimethylethyl)-4-(5-methoxy-2-benzoxazolyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29078-05-5

Post Buying Request

29078-05-5 Suppliers

Recommended suppliers

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

29078-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29078-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,7 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29078-05:
(7*2)+(6*9)+(5*0)+(4*7)+(3*8)+(2*0)+(1*5)=125
125 % 10 = 5
So 29078-05-5 is a valid CAS Registry Number.

29078-05-5Downstream Products

29078-05-5Relevant academic research and scientific papers

PRODUCTION METHOD OF 2-(HYDROXYPHENYL) BENZOXAZOLES

-

Paragraph 0037; 0041, (2016/12/07)

PROBLEM TO BE SOLVED: To provide a production method of 2-(hydroxyphenyl) benzoxazoles. SOLUTION: A method of producing 2-(hydroxyphenyl) benzoxazoles is characterized by reacting a 2-nitro phenol compound having, in a molecule, at least one a benzene ring substituted with a hydroxyl group at one and a nitro group at the other of mutually adjacent carbon atoms or a condensed polycyclic hydrocarbon ring comprising the benzene ring, with a methyl phenol compound having a benzene ring substituted with a methyl group and a hydroxyl group. COPYRIGHT: (C)2015,JPOandINPIT

Redox-neutral iron-sulfur promoted transformation of 2-nitrophenols and 2,6-disubstituted p -cresols into 2-arylbenzoxazoles

Saibara, Masahiko,Ashida, Kazuhito,Satomi, Kouji,Iwai, Toshiyuki,Nakai, Takeo,Mihara, Masatoshi,Ito, Takatoshi,Mizuno, Takumi

supporting information, p. 1565 - 1570 (2014/07/08)

A catalyst based on iron and elemental sulfur has been shown to efficiently promote a redox-neutral reaction between 2-nitrophenols and 2,6-disubstituted p-cresols, allowing for the preparation of 2-arylbenzoxazoles in good yields. This synthetic methodology also affords high atom economy without the use of any external oxidizing and/or reducing reagents. This is the first redox-condensation reaction of 2-nitrophenols with 2,6-disubstituted p-cresols. Georg Thieme Verlag Stuttgart New York.

NOVEL COMPOUNDS USEFUL AS NEURO-PROTECTIVE AGENTS

-

, (2008/06/13)

This invention relates to novel phenyl oxazoles, thiazoles, oxazolines, oxadiazoles and benzoxazoles useful as neuro-protective agents.

Compounds useful as neuro-protective agents

-

, (2008/06/13)

This invention relates to novel phenyl oxazoles, thiazoles, oxazolines, oxadiazoles and benzoxazoles useful as neuro-protective agents.

Studies on the synthesis and anti-inflammatory activity of 2,6-Di-tert-butylphenols with a heterocyclic group at the 4-position I

Isomura, Yasuo,Ito, Noriki,Homma, Hiroshige,Abe, Tetsushi,Kubo, Kazuo

, p. 3168 - 3178 (2007/10/02)

A number of 2,6-di-tert-butylphenols with a heterocyclic group at the 4-position were prepared. The heterocyclic groups were as follows: benzoxazole, benzothiazole, benzimidazole, indole, imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrimidine. Anti-inflammat

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 29078-05-5