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(4S,4aR,8aR)-4-(furan-3-yl)-3-methyl-8a-[(trimethylsilyl)oxy]-4a,5,6,7,8,8a-hexahydro-4H-1,2-benzoxazine 2-oxide is a complex organic compound characterized by the presence of a furan ring, a methyl group, and a benzoxazine ring with a trimethylsilyl group attached. (4S,4aR,8aR)-4-(furan-3-yl)-3-methyl-8a-[(trimethylsilyl)oxy]-4a,5,6,7,8,8a-hexahydro-4H-1,2-benzoxazine 2-oxide also features an oxygen atom in the benzoxazine ring, which designates it as a 2-oxide. The stereochemistry of its chiral centers is indicated by the 4S, 4aR, 8aR configuration. Due to its unique structure and functional groups, (4S,4aR,8aR)-4-(furan-3-yl)-3-methyl-8a-[(trimethylsilyl)oxy]-4a,5,6,7,8,8a-hexahydro-4H-1,2-benzoxazine 2-oxide holds potential applications in the fields of organic synthesis and medicinal chemistry.

124070-89-9

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124070-89-9 Usage

Uses

Used in Organic Synthesis:
(4S,4aR,8aR)-4-(furan-3-yl)-3-methyl-8a-[(trimethylsilyl)oxy]-4a,5,6,7,8,8a-hexahydro-4H-1,2-benzoxazine 2-oxide is used as a key intermediate for the synthesis of various complex organic molecules. Its unique structure and functional groups make it a valuable building block in the creation of novel compounds with potential applications in various industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4S,4aR,8aR)-4-(furan-3-yl)-3-methyl-8a-[(trimethylsilyl)oxy]-4a,5,6,7,8,8a-hexahydro-4H-1,2-benzoxazine 2-oxide is used as a starting material for the development of new pharmaceuticals. Its structural diversity and the presence of multiple functional groups allow for the design and synthesis of bioactive molecules with potential therapeutic properties.
Used in Pharmaceutical Industry:
(4S,4aR,8aR)-4-(furan-3-yl)-3-methyl-8a-[(trimethylsilyl)oxy]-4a,5,6,7,8,8a-hexahydro-4H-1,2-benzoxazine 2-oxide is used as a precursor in the synthesis of new drugs for the treatment of various diseases. Its unique structural features and functional groups can be exploited to develop molecules with improved pharmacological properties, such as enhanced potency, selectivity, and bioavailability.
Used in Chemical Research:
In the realm of chemical research, (4S,4aR,8aR)-4-(furan-3-yl)-3-methyl-8a-[(trimethylsilyl)oxy]-4a,5,6,7,8,8a-hexahydro-4H-1,2-benzoxazine 2-oxide serves as a model compound for studying the reactivity and chemical behavior of complex organic molecules. Its unique structure and functional groups provide valuable insights into the underlying principles governing organic reactions and can contribute to the advancement of synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 124070-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,7 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124070-89:
(8*1)+(7*2)+(6*4)+(5*0)+(4*7)+(3*0)+(2*8)+(1*9)=99
99 % 10 = 9
So 124070-89-9 is a valid CAS Registry Number.

124070-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [(4S,4aR,8aR)-4-(furan-3-yl)-3-methyl-2-oxido-4,4a,5,6,7,8-hexahydro-1,2-benzoxazin-2-ium-8a-yl]oxy-trimethylsilane

1.2 Other means of identification

Product number -
Other names 4H-1,2-Benzoxazine,4-(3-furanyl)-4a,5,6,7,8,8a-hexahydro-3-methyl-8a-((trimethylsilyl)oxy)-,2-oxide,(4alpha,4aalpha,8abeta)

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:124070-89-9 SDS

124070-89-9Relevant academic research and scientific papers

Stereoselective Addition of Enol Silanes to Nitro Olefins. A Simple Synthesis of Compounds Related to the Insect Antifeedants Azadiradion and Gedunin.

Mateos, A. Fernandez,Fuente Blanco, Jesus A. de la

, p. 1349 - 1354 (2007/10/02)

The Lewis acid mediated aldol reactions of 1-cyclohexene (2) and 2,6,6-trimethyl-1-cyclohexene (6) with (E)-1-(3-furyl)-2-nitro-1-propene (1) was investigated (Schemes I and II and Chart II).The addition of enol s

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