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BENZYL 5-AMINO-4-[(TERT-BUTOXYCARBONYL)AMINO]-5-OXOPENTANOATE is a chemical compound that features a benzyl group attached to a pentanoate molecule, incorporating an amino group and a tert-butoxycarbonyl group. BENZYL 5-AMINO-4-[(TERT-BUTOXYCARBONYL)AMINO]-5-OXOPENTANOATE plays a significant role in organic synthesis and pharmaceutical research, serving as a versatile building block for the development of a wide range of compounds and drugs.

292870-04-3

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292870-04-3 Usage

Uses

Used in Organic Synthesis:
BENZYL 5-AMINO-4-[(TERT-BUTOXYCARBONYL)AMINO]-5-OXOPENTANOATE is used as a key intermediate in organic synthesis for the creation of various organic compounds. Its unique structure allows for multiple points of chemical modification, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, BENZYL 5-AMINO-4-[(TERT-BUTOXYCARBONYL)AMINO]-5-OXOPENTANOATE is utilized as a building block for the development of new drugs. Its presence in the molecular structure can contribute to the pharmacological properties of the final drug product, potentially enhancing efficacy, selectivity, or stability.
Used as a Protecting Group in Organic Chemistry:
The tert-butoxycarbonyl group in BENZYL 5-AMINO-4-[(TERT-BUTOXYCARBONYL)AMINO]-5-OXOPENTANOATE is commonly used as a protecting group for amines during organic synthesis. This feature allows chemists to temporarily mask the reactivity of the amine group, facilitating selective reactions at other sites within the molecule.
Used as a Protecting Group for Alcohols in Chemical Synthesis:
Similarly, the benzyl group serves as a common protecting group for alcohols in chemical synthesis. This protects the hydroxyl group from unwanted reactions, ensuring that the desired transformations occur at specific sites within the molecule.
Overall, BENZYL 5-AMINO-4-[(TERT-BUTOXYCARBONYL)AMINO]-5-OXOPENTANOATE is an important intermediate in the production of various pharmaceuticals and organic compounds, playing a crucial role in both the synthesis of new molecules and the protection of functional groups during chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 292870-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,8,7 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 292870-04:
(8*2)+(7*9)+(6*2)+(5*8)+(4*7)+(3*0)+(2*0)+(1*4)=163
163 % 10 = 3
So 292870-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H24N2O5/c1-17(2,3)24-16(22)19-13(15(18)21)9-10-14(20)23-11-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H2,18,21)(H,19,22)/t13-/m1/s1

292870-04-3SDS

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 BENZYL 5-AMINO-4-[(TERT-BUTOXYCARBONYL)AMINO]-5-OXOPENTANOATE

1.2 Other means of identification

Product number -
Other names (S)-Benzyl 4-amino-5-(aminocarbonyl)pentanoate,N4-BOC protected

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:292870-04-3 SDS

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