Welcome to LookChem.com Sign In|Join Free

CAS

  • or
(1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid is a complex chemical compound derived from the bicyclic structure of azabicyclohexane, featuring a carboxylic acid and a tert-butoxycarbonyl group attached to specific carbon atoms. Its unique molecular configuration and functional groups suggest potential pharmaceutical and medicinal applications, with the carboxylic acid group possibly interacting with biological receptors or enzymes, and the tert-butoxycarbonyl group serving as a protective group in organic synthesis.

927679-54-7 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • (1R,5S,6R)-3-(TERT-BUTOXYCARBONYL)-3-AZABICYCLO[3.1.0]HEXANE-6-CARBOXYLIC ACID

    Cas No: 927679-54-7

  • USD $ 1.9-2.9 / Gram

  • 100 Gram

  • 1000 Metric Ton/Month

  • Chemlyte Solutions
  • Contact Supplier
  • 927679-54-7 Structure
  • Basic information

    1. Product Name: (1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid
    2. Synonyms: (1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid;cis-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid;(1alpha,5alpha,6alpha)-3-Azabicyclo[3.1.0]hexane-3,6-dicarboxylic acid 3-(tert-butyl) ester;exo-3-Boc-3-azabicyclo[3.1.0]hexane-6-carboxylic acid;exo-3-Boc-3-azabicyclo[3....;(1R*,5S*,6r*)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid(SALTDATA: FREE);3-Azabicyclo[3.1.0]hexane-3,6-dicarboxylic acid, 3-(1,1-diMethylethyl) ester, (1,5,6)/Cis-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylicacid;3-Azabicyclo[3.1.0]hexane-3,6-dicarboxylic acid, 3-(1,1-diMethylethyl) ester, (1á,5á,6á)/Cis-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylicacid
    3. CAS NO:927679-54-7
    4. Molecular Formula: C11H17NO4
    5. Molecular Weight: 227.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 927679-54-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 355.9 °C at 760 mmHg
    3. Flash Point: 169 °C
    4. Appearance: /
    5. Density: 1.276
    6. Vapor Pressure: 5.03E-06mmHg at 25°C
    7. Refractive Index: 1.537
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 4.56±0.20(Predicted)
    11. CAS DataBase Reference: (1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: (1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid(927679-54-7)
    13. EPA Substance Registry System: (1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid(927679-54-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 927679-54-7(Hazardous Substances Data)

927679-54-7 Usage

Uses

Used in Pharmaceutical Industry:
(1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid is used as a potential pharmaceutical agent for its unique structure and functional groups, which may allow it to interact with biological receptors or enzymes, contributing to the development of new drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid is utilized for its potential to be further modified or used as a building block in the synthesis of new medicinal compounds, given its specific molecular features.
Used in Organic Synthesis:
(1R,5S,6R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid is employed as a protecting group in organic synthesis, where the tert-butoxycarbonyl group can be selectively removed under mild conditions, facilitating the synthesis of more complex organic molecules.
Further research and testing are required to fully explore the properties and potential applications of this compound across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 927679-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,7,6,7 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 927679-54:
(8*9)+(7*2)+(6*7)+(5*6)+(4*7)+(3*9)+(2*5)+(1*4)=227
227 % 10 = 7
So 927679-54-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO4/c1-11(2,3)16-10(15)12-4-6-7(5-12)8(6)9(13)14/h6-8H,4-5H2,1-3H3,(H,13,14)/t6-,7+,8+

927679-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,5S,6r)-3-(tert-Butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names (1R,5S)-3-[(2-methylpropan-2-yl)oxycarbonyl]-3-azabicyclo[3.1.0]hexane-6-carboxylic acid

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:927679-54-7 SDS

927679-54-7Relevant articles and documents

ALKYNYL QUINAZOLINE COMPOUNDS

-

Paragraph 1159, (2021/02/19)

The present disclosure relates to compounds of Formula (I'): and pharmaceutically acceptable salts and stereoisomers thereof. The present disclosure also relates to methods of preparation these compounds, compositions comprising these compounds, and methods of using them in the prevention or treatment of abnormal cell growth in mammals, especially humans.

NOVEL 6-PYRAZOLYLAMIDO-3-SUBSTITUTED AZABICYCLO[3.1.0]HEXANE COMPOUNDS AS CALCIUM CHANNEL INHIBITORS

-

, (2014/12/09)

The present invention relates to a 6-pyrazolylamido-3-substituted azabicyclo[3.1.0]hexane derivatives useful as calcium channel blockers, pharmaceutically acceptable salts thereof and medical use of the calcium channel inhibiting effect of the compounds for treatment of diseases.

Novel GlyT1 inhibitor chemotypes by scaffold hopping. Part 1: Development of a potent and CNS penetrant [3.1.0]-based lead

Jones, Carrie K.,Sheffler, Douglas J.,Williams, Richard,Jadhav, Sataya B.,Felts, Andrew S.,Morrison, Ryan D.,Niswender, Colleen M.,Daniels, J. Scott,Conn, P. Jeffrey,Lindsley, Craig W.

, p. 1067 - 1070 (2014/03/21)

This Letter describes the development and SAR of a novel series of GlyT1 inhibitors derived from a scaffold hopping approach that provided a robust intellectual property position, in lieu of a traditional, expensive HTS campaign. Members within this new [3.1.0]-based series displayed excellent GlyT1 potency, selectivity, free fraction, CNS penetration and efficacy in a preclinical model of schizophrenia (prepulse inhibition).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 927679-54-7