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TERT-BUTYL [6-(2-AMINOETHYL)PYRIDIN-2-YL]CARBAMATE is a chemical compound with the molecular formula C14H22N4O2. It is an organic compound that belongs to the carbamate family and contains the tert-butyl group and an aminoethylpyridinyl group. TERT-BUTYL [6-(2-AMINOETHYL)PYRIDIN-2-YL]CARBAMATE may be utilized in research and development or manufacturing processes across various industries. Due to its chemical nature, it is crucial to handle TERT-BUTYL [6-(2-AMINOETHYL)PYRIDIN-2-YL]CARBAMATE with care and adhere to proper safety protocols to mitigate potential health and environmental risks.

400776-37-6

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400776-37-6 Usage

Uses

Used in Pharmaceutical Research and Development:
TERT-BUTYL [6-(2-AMINOETHYL)PYRIDIN-2-YL]CARBAMATE is used as a research compound for the development of new pharmaceuticals. Its unique structure, which includes the carbamate group and the aminoethylpyridinyl group, may offer specific biological activities or interactions with biological targets, making it a candidate for drug discovery and medicinal chemistry.
Used in Chemical Synthesis:
In the chemical industry, TERT-BUTYL [6-(2-AMINOETHYL)PYRIDIN-2-YL]CARBAMATE is used as an intermediate in the synthesis of other organic compounds. Its versatile structure allows for further functionalization and modification, which can lead to the creation of new molecules with desired properties for various applications.
Used in Material Science:
TERT-BUTYL [6-(2-AMINOETHYL)PYRIDIN-2-YL]CARBAMATE may also find applications in material science, where it could be used to develop new materials with specific properties. Its incorporation into polymers or other materials could potentially enhance their performance or introduce new functionalities.
Used in Analytical Chemistry:
As a compound with distinct chemical characteristics, TERT-BUTYL [6-(2-AMINOETHYL)PYRIDIN-2-YL]CARBAMATE can be employed in analytical chemistry for the development of new methods or techniques for detecting, quantifying, or analyzing other substances.

Check Digit Verification of cas no

The CAS Registry Mumber 400776-37-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,7,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 400776-37:
(8*4)+(7*0)+(6*0)+(5*7)+(4*7)+(3*6)+(2*3)+(1*7)=126
126 % 10 = 6
So 400776-37-6 is a valid CAS Registry Number.

400776-37-6SDS

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 tert-butyl N-[6-(2-aminoethyl)pyridin-2-yl]carbamate

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:400776-37-6 SDS

400776-37-6Relevant articles and documents

Benzamide compounds as apo b secretion inhibitors

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, (2008/06/13)

The present invention relates to compounds of the formula (I) wherein R1 and R2 are each independently lower alkyl lower alkenyl, acyl, amino, lower alkoxy, lower cycloalkyloxy, aryl, aryloxy, sulfooxy, mercapto, sulfo, hydrogen, halogen, nitro, cyano or hydroxy, or may form a ring structure; Q1 is N or CH; L is optionally substituted unsaturated 3 to 10-membered heterocyclic group; X is optionally substituted monocyclic arylene or monocyclic heteroarylene; Y is -(A1)m-(A2)n-(A4)k-; Z is directbond, —CH2-, —NH— or —O—; and R is hydrogen or lower alkyl, or a salt thereof The compounds of the present invention inhibit apolipoprotein B (Apo B) secretion and are useful as a medicament for prophylactic and treatment of diseases or conditions resulting from elevated circulating levels of Apo B.

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