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Tert-butyl (cis-3-aminocyclobutyl)carbamate is a specialized chemical compound characterized by its cyclobutyl ring structure, an amino group (NH2), and a carbamate function (OC(O)NR2). The "cis" prefix indicates the specific configuration of the atoms around the cyclobutyl ring, with two particular atoms or groups positioned on the same side. Additionally, the molecule features a tertiary butyl group attached to it. Due to its potentially reactive nature, this chemical requires careful handling using precise scientific techniques, primarily in scientific research or pharmaceutical settings.

1212395-34-0

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1212395-34-0 Usage

Uses

Used in Scientific Research:
Tert-butyl (cis-3-aminocyclobutyl)carbamate is utilized as a research compound for studying its chemical properties and potential applications in various scientific fields. Its unique molecular structure, including the cyclobutyl ring, amino group, and carbamate function, makes it a valuable subject for investigation.
Used in Pharmaceutical Development:
In the pharmaceutical industry, tert-butyl (cis-3-aminocyclobutyl)carbamate serves as a key intermediate or building block in the synthesis of various drug molecules. Its reactive nature and specific molecular configuration allow it to be incorporated into the development of new pharmaceutical compounds with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 1212395-34-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,2,3,9 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1212395-34:
(9*1)+(8*2)+(7*1)+(6*2)+(5*3)+(4*9)+(3*5)+(2*3)+(1*4)=120
120 % 10 = 0
So 1212395-34-0 is a valid CAS Registry Number.

1212395-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name cis tert-Butyl N-(3-aminocyclobutyl)carbamate

1.2 Other means of identification

Product number -
Other names (6-OXOSPIRO[3.3]HEPT-2-YL)CARBAMIC ACID TERT-BUTYL ESTER

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:1212395-34-0 SDS

1212395-34-0Downstream Products

1212395-34-0Relevant articles and documents

HETEROBICYCLIC COMPOUNDS

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, (2013/09/12)

Heterobicyclic compounds of Formula (I): or a pharmaceutically-acceptable salt, tautomer, or stereoisomer thereof, as defined in the specification, and compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treating disorders or diseases treatable by inhibition of PDE10, such as obesity, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, Huntington's Disease, and the like.

Cyclobutane-derived diamines: Synthesis and molecular structure

Radchenko, Dmytro S.,Pavlenko, Sergiy O.,Grygorenko, Oleksandr O.,Volochnyuk, Dmitriy M.,Shishkina, Svitlana V.,Shishkin, Oleg V.,Komarov, Igor V.

experimental part, p. 5941 - 5952 (2010/11/04)

Cyclobutane diamines (i.e., cis- and trans-1,3-diaminocyclobutane, 6-amino-3-azaspiro[3.3]heptane, and 3,6-diaminospiro[3.3]heptane) are considered as promising sterically constrained diamine building blocks for drug discovery. An approach to the syntheses of their Boc-monoprotected derivatives has been developed aimed at the preparation of multigram amounts of the compounds. These novel synthetic schemes exploit classical malonate alkylation chemistry for the construction of cyclobutane rings. The conformational preferences of the cyclobutane diamine derivatives have been evaluated by X-ray diffraction and compared with the literature data on sterically constrained diamines, which are among the constituents of commercially available drugs.

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