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(4R)-4-(1,1-dimethylethyl)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-oxazole is a chiral oxazole derivative with the molecular formula C27H31NOP. It features a phosphino-substituted phenyl group and is known for its unique structure and properties. This chemical compound is a valuable intermediate in the development of various chemical and pharmaceutical products due to its potential applications in organometallic chemistry, catalysis, and pharmaceutical research.

164858-79-1

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164858-79-1 Usage

Uses

Used in Organometallic Chemistry:
(4R)-4-(1,1-diMethylethyl)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-Oxazole is used as a ligand for organometallic chemistry applications. Its phosphino-substituted phenyl group allows it to form stable complexes with metal centers, facilitating various chemical reactions and transformations.
Used in Catalysis:
In the field of catalysis, (4R)-4-(1,1-diMethylethyl)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-Oxazole serves as a catalyst or a catalyst precursor. Its unique structure enables it to promote a wide range of chemical reactions, enhancing their efficiency and selectivity.
Used in Pharmaceutical Research:
(4R)-4-(1,1-diMethylethyl)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-Oxazole is used as a building block in pharmaceutical research for the synthesis of new compounds with potential biological activity. Its chiral oxazole framework and phosphino-substituted phenyl group provide a versatile platform for the development of novel therapeutic agents.
Used in Chemical Product Development:
(4R)-4-(1,1-diMethylethyl)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-Oxazole is utilized as an intermediate in the development of various chemical products. Its unique structure and properties make it a valuable component in the synthesis of advanced materials, specialty chemicals, and other high-value products.

Check Digit Verification of cas no

The CAS Registry Mumber 164858-79-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,8,5 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 164858-79:
(8*1)+(7*6)+(6*4)+(5*8)+(4*5)+(3*8)+(2*7)+(1*9)=181
181 % 10 = 1
So 164858-79-1 is a valid CAS Registry Number.

164858-79-1SDS

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 (R)-Stoltz ligand

1.2 Other means of identification

Product number -
Other names (R)-t-Bu-PHOX

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:164858-79-1 SDS

164858-79-1Downstream Products

164858-79-1Relevant academic research and scientific papers

Total Synthesis of the Alleged Structure of Crenarchaeol Enables Structure Revision**

Cunha, Ana V.,Havenith, Remco W. A.,Holzheimer, Mira,Minnaard, Adriaan J.,Schouten, Stefan,Sinninghe Damsté, Jaap S.

, p. 17504 - 17513 (2021/07/06)

Crenarchaeol is a glycerol dialkyl glycerol tetraether lipid produced exclusively in Archaea of the phylum Thaumarchaeota. This membrane-spanning lipid is undoubtedly the structurally most sophisticated of all known archaeal lipids and an iconic molecule in organic geochemistry. The 66-membered macrocycle possesses a unique chemical structure featuring 22 mostly remote stereocenters, and a cyclohexane ring connected by a single bond to a cyclopentane ring. Herein we report the first total synthesis of the proposed structure of crenarchaeol. Comparison with natural crenarchaeol allowed us to propose a revised structure of crenarchaeol, wherein one of the 22 stereocenters is inverted.

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