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(1S,2S,5R)-6,6-diMethyl-3-azabicyclo, a member of the azabicyclic class of compounds, is a unique chemical entity characterized by its 3-azabicyclo[3.1.0]hexane core. This core is adorned with two methyl groups at the 1 and 2 positions, and an additional methyl group at the 5 position. The stereochemistry of (1S,2S,5R)-6,6-diMethyl-3-azabicyclo is defined by its specific three-dimensional arrangement of substituents, which is indicated by the (1S,2S,5R) designation. (1S,2S,5R)-6,6-diMethyl-3-azabicyclo is often utilized as an intermediate in the synthesis of pharmaceuticals, and its distinctive structure and stereochemistry may endow it with intriguing pharmacological or chemical properties. These attributes render (1S,2S,5R)-6,6-diMethyl-3-azabicyclo a potentially valuable asset for drug development and as a research tool in chemical synthesis.

911835-76-2

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911835-76-2 Usage

Uses

Used in Pharmaceutical Synthesis:
(1S,2S,5R)-6,6-diMethyl-3-azabicyclo is employed as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and stereochemistry allow it to serve as a key building block in the creation of new medicinal compounds, potentially leading to the development of innovative treatments for a range of diseases and conditions.
Used in Drug Development:
Due to its potential pharmacological properties, (1S,2S,5R)-6,6-diMethyl-3-azabicyclo is used in drug development to explore its therapeutic potential. Researchers may investigate its interactions with biological targets, such as enzymes or receptors, to assess its efficacy and safety as a candidate for new drug therapies.
Used in Chemical Synthesis Research:
(1S,2S,5R)-6,6-diMethyl-3-azabicyclo also serves as a research tool in chemical synthesis. Its distinctive structure provides a platform for studying various synthetic pathways and reaction mechanisms, which can contribute to the advancement of synthetic chemistry and the discovery of new synthetic methods.
Used in Stereochemistry Studies:
The specific stereochemistry of (1S,2S,5R)-6,6-diMethyl-3-azabicyclo makes it a valuable subject for stereochemistry studies. Understanding the impact of stereochemistry on the compound's properties and reactivity can provide insights into the design of enantioselective syntheses and the development of chiral molecules with specific biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 911835-76-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,8,3 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 911835-76:
(8*9)+(7*1)+(6*1)+(5*8)+(4*3)+(3*5)+(2*7)+(1*6)=172
172 % 10 = 2
So 911835-76-2 is a valid CAS Registry Number.

911835-76-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S,5S)-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxylic acid

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 -
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More Details:911835-76-2 SDS

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