181657-56-7 Usage
Description
(1R,2R)-(-)-2-Benzyloxycyclopentylamine is an organic compound characterized by its specific stereochemistry and functional groups. It is a chiral amine derivative with a cyclopentyl ring and a benzyloxy substituent, which contributes to its unique chemical properties and reactivity.
Uses
(1R,2R)-(-)-2-Benzyloxycyclopentylamine is used as a key intermediate in the synthesis of various complex organic molecules and pharmaceuticals. Its unique structure allows it to be a versatile building block for the development of new drugs and other chemical products.
Used in Pharmaceutical Industry:
(1R,2R)-(-)-2-Benzyloxycyclopentylamine is used as a raw material for the development of new drugs. Its specific stereochemistry and functional groups make it a valuable component in the design and synthesis of novel pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
(1R,2R)-(-)-2-Benzyloxycyclopentylamine is used as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique properties can be exploited to create new compounds with improved efficacy and selectivity in controlling pests and weeds.
Used in Dyestuff Industry:
(1R,2R)-(-)-2-Benzyloxycyclopentylamine is used as a starting material for the production of various dyes and pigments. Its chemical structure can be modified to create new colorants with specific properties, such as improved color strength, stability, and solubility.
Used in Organic Synthesis:
(1R,2R)-(-)-2-Benzyloxycyclopentylamine is used as a versatile intermediate in organic synthesis, allowing for the creation of a wide range of chemical products. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 181657-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,6,5 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 181657-56:
(8*1)+(7*8)+(6*1)+(5*6)+(4*5)+(3*7)+(2*5)+(1*6)=157
157 % 10 = 7
So 181657-56-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c13-11-7-4-8-12(11)14-9-10-5-2-1-3-6-10/h1-3,5-6,11-12H,4,7-9,13H2/t11-,12-/m1/s1
181657-56-7Relevant articles and documents
Hybrid Organo- and Biocatalytic Process for the Asymmetric Transformation of Alcohols into Amines in Aqueous Medium
Liardo, Elisa,Ríos-Lombardía, Nicolás,Morís, Francisco,Rebolledo, Francisca,González-Sabín, Javier
, p. 4768 - 4774 (2017/07/24)
A hybrid organo- and biocatalytic system for the asymmetric conversion of racemic alcohols into amines was developed. Combining an organocatalyst, AZADO, an oxidant, NaOCl, and an enzyme, ω-transaminase, we implemented a one-pot oxidation-transamination sequential process in aqueous medium. The method showed broad substrate scope and was successfully applied to conventional secondary alcohols and sterically hindered β-substituted cycloalkanols, where a highly stereoselective dynamic asymmetric bioamination enabled us to set up both contiguous stereocenters with very high enantio- and diastereomeric ratio (>90% yield, >99% ee, and up to 49:1 dr).
COMBINATION OF BENZOTHIAZOL-2-ONE BETA2 ADRENOCEPTOR AGONISTS AND CORTICOSTEROIDS FOR THE TREATMENT OF RESPIRATORY DISEASES
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Page/Page column 30, (2010/02/13)
A medicament comprising, separately or together, (A) a compound of Formula (I) in free or salt or solvate form, wherein X has the meaning as indicated in the specification; and (B) a corticosteroid, for simultaneous, sequential or separate administration in the treatment of an inflammatory obstructive airways disease, the molar ratio of (A) to (B) being from 100:1 to 1:300.
