202752-01-0

Basic information

• Product Name: (R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate
• Synonyms: (R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate
• CAS NO: 202752-01-0
• Molecular Weight: 584.739
• Mol File: 202752-01-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate(202752-01-0)
• EPA Substance Registry System: (R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate(202752-01-0)

Safety Data

• Hazardous Substances Data: 202752-01-0(Hazardous Substances Data)

Usage

Description

(R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate is a complex organic chemical compound characterized by its fluorenyl methyl and propan-2-ylcarbamate groups, along with a distinctive (1-amino-1-oxo-3-(triphenylmethylthio) substituent. This unique molecular structure suggests potential applications in various fields, including pharmaceuticals, materials science, and biotechnology, although further research is required to explore its full potential.

Uses

Used in Pharmaceutical Industry:
(R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate is used as a potential pharmaceutical compound for its unique structure and reactivity, which may offer novel therapeutic applications.
Used in Materials Science:
In the field of materials science, (R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate could be utilized as a component in the development of new materials with specific properties, such as improved stability or reactivity.
Used in Biotechnology:
(R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate may also find applications in biotechnology, where its unique chemical properties could be harnessed for the creation of new bioactive molecules or as part of biocompatible materials for medical applications.

Upstream product

• 103213-32-7 N-(9-fluorenylmethoxycarbonyl)-S-trityl-L-cysteine 

Downstream Products

• 166737-85-5 (2R)-2-Amino-3-(tritylsulfanyl)propanamide 

Relevant articles and documents

Synthesis method of S-trityl-L-cysteinamide

The invention relates to a synthesis method of S-trityl-L-cysteinamide. The method mainly solves the technical problem of product racemization in the existing synthesis method. The preparation method comprises the following three steps: step 1, adding CDI into a tetrahydrofuran solution of (+)-S-trityl-L-cysteine, stirring to react for 4 hours, and adding ammonia water to obtain a compound 1; 2, the compound 1 reacts with piperidine in N, N-dimethylformamide to obtain a compound 2; and 3, dissolving the compound 2 in ethyl acetate, adding L-dibenzoyl tartaric acid to form salt, measuring that ee is greater than 99.0%, and alkalifying to obtain a pure compound 3.

Aminothiol compound, preparation method of aminothiol compound and application of aminothiol compound in radiation protection

The invention discloses an aminothiol compound, a preparation method of the aminothiol compound and application of the aminothiol compound in radiation protection. The compound has a structure shown in the formula I in the description, wherein A1 is selected from -C(O)NR8-, -S(O)2-NR8-, -S(O)NR8- and -R7-NR8-, A2 is selected from carbonyl, sulfonyl, sulfinyl and substituted or unsubstituted C1-6 alkyl, R1, R2, R5 and R6 can be the same or not and are selected from hydrogen and substituted or unsubstituted C1-C5 alkyl or hetero alkyl, n is an integer from 0 to 20000, R3 and R4 are independently selected from hydrogen, X and substituted or unsubstituted C1-6 alkyl, X is selected from F, Cl, Br and I, R7 is selected from substituted or unsubstituted C1-C6 alkyl, and R8 is selected from hydrogen and substituted or unsubstituted C1-C6 alkyl. The compound has the effect of reducing biological injury caused by ionizing radiation and also has the effects of prolonging the lifetime of radiated animals and increasing the survival rate of the radiated animals.