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174456-77-0

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174456-77-0 Usage

General Description

Ethyl 3-azabicyclo[3.1.0]hexane-6-carboxylate is a chemical compound with a unique and complex structure. It is a derivative of the azabicyclo[3.1.0]hexane ring system and contains an ethyl ester functional group. Ethyl 3-azabicyclo[3.1.0]hexane-6-carboxylate has potential applications in medicinal chemistry as a building block for the synthesis of pharmaceuticals and bioactive compounds. Its stable and rigid structure makes it an interesting target for chemical synthesis and structural modification. Overall, Ethyl 3-azabicyclo[3.1.0]hexane-6-carboxylate is a versatile and valuable chemical compound with various potential uses in the field of chemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 174456-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,4,5 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 174456-77:
(8*1)+(7*7)+(6*4)+(5*4)+(4*5)+(3*6)+(2*7)+(1*7)=160
160 % 10 = 0
So 174456-77-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c1-2-11-8(10)7-5-3-9-4-6(5)7/h5-7,9H,2-4H2,1H3

174456-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (1R*,5S*,6r*)-3-azabicyclo[3.1.0]hexane-6-carboxylate(SALTDATA: HCl)

1.2 Other means of identification

Product number -
Other names -

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:174456-77-0 SDS

174456-77-0Relevant articles and documents

Synthesis and diacylglycerol acyltransferase-1 inhibition of azabicyclo[3.1.0]hexane derivatives

Han, Seo-Jung,Lee, Gwi Bin,Kwak, Hyun Jung,Pagire, Suvarna H.,Kim, Ji Young,Pagire, Haushabhau S.,Park, Sung Bum,Chae, Chong Hak,Lee, Joo Yun,Kim, Ki Young,Rhee, Sang Dal,Kim, Hee Youn,Shin, Sun Hye,Bae, Myung Ae,Park, Mi-Jin,Kim, Dooseop,Lee, Duck Hyung,Ahn, Jin Hee

, p. 1586 - 1593 (2015/07/15)

We identified azabicyclo[3.1.0]hexane derivatives that are active diacylglycerol acyltransferase-1 (DGAT)-1 inhibitor. Among the azabicyclo[3.1.0]hexane series, compound 6b showed good in vitro activity toward human DGAT-1, selectivity toward DGAT-2, and

BENZODIOXANE INHIBITORS OF LEUKOTRIENE PRODUCTION FOR COMBINATION THERAPY

-

Paragraph 0348, (2013/09/26)

The present invention relates to a combination comprising compounds of formula (I): wherein R1 to R3, A, X and n are as defined herein, and an additional active agent. The present invention also relates to pharmaceutical compositions comprising these combinations, and methods of using these combinations to treat various diseases and disorders.

SUBSTITUTED 3-AZABICYCLO[3.1.0]HEXANE DERIVATIVES USEFUL AS CCR2 ANTAGONISTS

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, (2012/10/07)

Disclosed are CCR2 antagonists of Formula (I)or pharmaceutically acceptable thereof, wherein R1, L1 and A are defined herein. Also disclosed are pharmaceutical compositions containing the compounds, methods of treatment using the compounds, and compositions to treat diseases or disorders associated with CCR2 activity.

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