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(5S,5'S,10S,10'R)-N,N'-(1,5-Pentanediyl)bis[7,9-dibromo-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide] is a complex spirocyclic molecule with a unique stereochemistry specified by the (5S,5'S,10S,10'R) prefix. It features multiple bromine atoms, hydroxyl groups, a methoxy group, and an amide functional group, all connected by a pentanediyl linker. This diverse functionalization and intricate structure potentially endow the compound with a broad spectrum of chemical and biological properties.

34232-66-1

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34232-66-1 Usage

Uses

Used in Pharmaceutical Industry:
(5S,5'S,10S,10'R)-N,N'-(1,5-Pentanediyl)bis[7,9-dibromo-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide] is used as a pharmaceutical agent for its potential therapeutic effects. (5S,5'S,10S,10'R)-N,N'-(1,5-Pentanediyl)bis[7,9-dibromo-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide]'s diverse functional groups and complex structure may contribute to its interaction with various biological targets, offering opportunities for the development of new drugs with unique mechanisms of action.
Used in Chemical Research:
In the field of chemical research, (5S,5'S,10S,10'R)-N,N'-(1,5-Pentanediyl)bis[7,9-dibromo-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide] serves as a subject of study for understanding the properties and reactivity of complex spirocyclic molecules. Its unique structure and functional groups provide a platform for exploring new chemical reactions and synthesis pathways.
Used in Material Science:
(5S,5'S,10S,10'R)-N,N'-(1,5-Pentanediyl)bis[7,9-dibromo-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide] is utilized in material science for the development of novel materials with specific properties. (5S,5'S,10S,10'R)-N,N'-(1,5-Pentanediyl)bis[7,9-dibromo-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide]'s structural features and functional groups may be harnessed to create materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials with unique mechanical, electronic, or optical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 34232-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,3 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34232-66:
(7*3)+(6*4)+(5*2)+(4*3)+(3*2)+(2*6)+(1*6)=91
91 % 10 = 1
So 34232-66-1 is a valid CAS Registry Number.

34232-66-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name HOMOAEROTHIONIN (AN)

1.2 Other means of identification

Product number -
Other names (5S,5'S,10S,10'R)-N,N'-(1,5-Pentanediyl)bis[7,9-dibromo-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxamide]

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:34232-66-1 SDS

34232-66-1Downstream Products

34232-66-1Relevant academic research and scientific papers

Total syntheses of (±)-aerothionin, (±)-homoaerothionin, and (±)-aerophobin-1

Nishiyama,Yamamura

, p. 3453 - 3456 (2007/10/02)

(±)-Aerothionin, (±)-homoaerothionin, and (±)-aerophobin-1 have been successfully synthesized using phenolic oxidation of the methyl pyruvate oxime derivative with thallium(III) trifluoroacetate as a key step. The stereostructure of aerophobin-2 has been also established by comparison of the 1H NMR spectrum with those of related compounds.

TOTAL SYNTHESES OF (+/-)-AEROTHIONIN AND (+/-)-HOMOAEROTHIONIN

Nishiyama, Shigeru,Yamamura, Shosuke

, p. 3351 - 3352 (2007/10/02)

Both aerothionin and homoaerothionin, the novel metabolites of the sponges Aplysina aerophoba, A. fistularis and Verongia thiona, have been synthesized in racemic form.

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