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913829-90-0

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  • Oxazole,2-[(1S)-7'-[bis(3,5-dimethylphenyl)phosphino]-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-inden]-7-yl]-4,5-dihydro-4-(phenylmethyl)-,(4S)-

    Cas No: 913829-90-0

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  • Oxazole,2-[(1S)-7'-[bis(3,5-dimethylphenyl)phosphino]-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-inden]-7-yl]-4,5-dihydro-4-(phenylmethyl)-,(4S)-

    Cas No: 913829-90-0

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913829-90-0 Usage

Description

Oxazole,2-[(1S)-7'-[bis(3,5-dimethylphenyl)phosphino]-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-inden]-7-yl]-4,5-dihydro-4-(phenylmethyl)-,(4S)is a complex chemical compound characterized by a unique molecular structure. It features an oxazole ring, which is a five-membered heterocyclic compound with one oxygen and one nitrogen atom. Additionally, it contains a spirobi[1H-inden] group, which is connected to a phosphino and phenylmethyl side chains. The (4S) designation specifies the stereochemistry of the molecule. This intricate structure and the presence of various functional groups may endow the compound with potential applications in organic synthesis, pharmaceuticals, or material science.

Uses

Used in Organic Synthesis:
Oxazole,2-[(1S)-7'-[bis(3,5-dimethylphenyl)phosphino]-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-inden]-7-yl]-4,5-dihydro-4-(phenylmethyl)-,(4S)can be utilized as a building block or intermediate in organic synthesis. Its unique structure and functional groups may allow for the development of novel compounds with specific properties and applications.
Used in Pharmaceutical Industry:
Due to its complex structure and the presence of various functional groups, Oxazole,2-[(1S)-7'-[bis(3,5-dimethylphenyl)phosphino]-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-inden]-7-yl]-4,5-dihydro-4-(phenylmethyl)-,(4S)may have potential applications in the pharmaceutical industry. It could be used as an active pharmaceutical ingredient (API) or as a key intermediate in the synthesis of drug candidates.
Used in Material Science:
The unique structure and functional groups of Oxazole,2-[(1S)-7'-[bis(3,5-dimethylphenyl)phosphino]-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-inden]-7-yl]-4,5-dihydro-4-(phenylmethyl)-,(4S)may also find applications in material science. It could be used in the development of new materials with specific properties, such as advanced polymers, coatings, or sensors.

Check Digit Verification of cas no

The CAS Registry Mumber 913829-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,8,2 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 913829-90:
(8*9)+(7*1)+(6*3)+(5*8)+(4*2)+(3*9)+(2*9)+(1*0)=190
190 % 10 = 0
So 913829-90-0 is a valid CAS Registry Number.

913829-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3S)-4-[(4S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]-3,3'-spirobi[1,2-dihydroindene]-4'-yl]-bis(3,5-dimethylphenyl)phosphane

1.2 Other means of identification

Product number -
Other names (S,S)-7-[4-(benzyl)oxazol-2-yl]-7'-di(3,5-dimethylphenyl)phosphinyl-1,1'-spirobiindane

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:913829-90-0 SDS

913829-90-0Downstream Products

913829-90-0Relevant articles and documents

Well-defined chiral spiro iridium/phosphine-oxazoline cationic complexes for highly enantioselective hydrogenation of imines at ambient pressure

Zhu, Shou-Fei,Xie, Jian-Bo,Zhang, Yong-Zhen,Li, Shen,Zhou, Qi-Lin

, p. 12886 - 12891 (2008/02/05)

New chiral phosphine-oxazoline ligands (7, SIPHOX) with a rigid and bulky spirobiindane scaffold were synthesized, starting with optically pure 7-diphenylphosphino-7′-trifluoromethanesulfonyloxyl-1,1′- spirobiindane, in four steps in 40-64% overall yield.

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