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2-(FMoc-aMino)-2-(1,1-dioxo-4-tetrahydrothiopyranyl)acetic Acid is a unique organic compound and a derivative of the amino acid glycine. It features an FMoc (9-fluorenylmethyloxycarbonyl) protecting group on the amino group and a 1,1-dioxo-4-tetrahydrothiopyranyl group, which together confer distinctive structural and functional properties. 2-(FMoc-aMino)-2-(1,1-dioxo-4-tetrahydrothiopyranyl)acetic Acid is recognized for its potential in the realms of organic chemistry and drug development, serving as a versatile building block for the creation of new chemical entities with possible biological activity.

369402-98-2

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369402-98-2 Usage

Uses

Used in Peptide Chemistry:
2-(FMoc-aMino)-2-(1,1-dioxo-4-tetrahydrothiopyranyl)acetic Acid is used as a building block in peptide chemistry for the synthesis of complex peptide sequences. Its FMoc protecting group allows for selective deprotection and coupling reactions, facilitating the stepwise assembly of peptides with high precision and yield.
Used in Pharmaceutical Compound Synthesis:
In the pharmaceutical industry, 2-(FMoc-aMino)-2-(1,1-dioxo-4-tetrahydrothiopyranyl)acetic Acid is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structural features contribute to the development of novel drugs with improved pharmacological properties, such as enhanced potency, selectivity, and bioavailability.
Used in Bioconjugation:
2-(FMoc-aMino)-2-(1,1-dioxo-4-tetrahydrothiopyranyl)acetic Acid is employed as a versatile linker in bioconjugation processes. Its functional groups enable the covalent attachment of biologically active molecules, such as peptides, proteins, or nucleic acids, to other molecules or surfaces. This allows for the creation of conjugates with tailored properties and applications in diagnostics, therapeutics, and biosensing.
Overall, 2-(FMoc-aMino)-2-(1,1-dioxo-4-tetrahydrothiopyranyl)acetic Acid's diverse applications across different industries underscore its importance as a valuable chemical entity in modern scientific research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 369402-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,9,4,0 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 369402-98:
(8*3)+(7*6)+(6*9)+(5*4)+(4*0)+(3*2)+(2*9)+(1*8)=172
172 % 10 = 2
So 369402-98-2 is a valid CAS Registry Number.

369402-98-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,1-dioxothian-4-yl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)acetic 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

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More Details:369402-98-2 SDS

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