10065-71-1

Usage

Uses

Used in Organic Chemistry:
N-TRITYLGLYCINE METHYL ESTER is used as a chemical intermediate for the synthesis of other relevant chemical compounds due to its stability and reactivity.
Used in Laboratory Settings:
N-TRITYLGLYCINE METHYL ESTER is used as a reagent in various chemical reactions, facilitating the production of desired compounds for research purposes.
Used in Industrial Applications:
N-TRITYLGLYCINE METHYL ESTER is used as a building block in the production of complex organic molecules, contributing to the development of new materials and products in the chemical industry.

Upstream product

• 5680-79-5 glycine ethyl ester hydrochloride 
• 76-83-5 trityl chloride 
• 637-96-7 sarcosine hydrochloride 

Downstream Products

• 116435-38-2 N-trityl-glycine hydrazide 
• 51871-25-1 N-(triphenylmethyl)glycine p-nitrophenyl ester 
• 5893-05-0 Trt-Gly 
• 174836-16-9 N-triphenylmethyl-2,2-dideuterioethanolamine 
• 51871-29-5 N-Tritylglycyl-DL-α-aminopropionitril 

Relevant academic research and scientific papers

SUBSTITUTED OXADIAZOLE CHEMICAL COMPOUND AND COMPOSITION CONTAINING SAID CHEMICAL COMPOUND AND USE THEREOF

Provided are a substituted oxadiazole chemical compound and composition containing said chemical compound and use thereof; said substituted oxadiazole chemical compound is the oxadiazole chemical compound as represented by formula (I), or its crystalline form, pharmaceutically acceptable salt, prodrug, stereoisomer, hydrate, or solvent compound. The disclosed substituted oxadiazole chemical compound and composition containing said chemical compound are capable of inhibiting indoleamine 2,3-dioxygenase; it also has better pharmacokinetic parameter attributes and is capable of improving the drug concentration of the chemical compound in an animal body, thus improving the therapeutic efficacy and safety of the drug.

A convenient method for preparation of α-imino carboxylic acid derivatives and application to the asymmetric synthesis of unnatural α-amino acid derivative

We describe herein a manganese(IV) oxide-mediated oxidation of N-p-methoxyphenyl (PMP)-protected glycine derivatives for the synthesis of α-imino carboxylic acid derivatives. Using this methodology, utilization of unstable glyoxic acid derivatives was avo

Derivatives and application to the asymmetric synthesis of unnatural α-amino acid derivative

We describe herein a manganese(IV) oxide-mediated oxidation of N-p-methoxyphenyl (PMP)-protected glycine derivatives for the synthesis of a-imino carboxylic acid derivatives. Using this methodology, utilization of unstable glyoxic acid derivatives was avoided. Furthermore, using this methodology we synthesized novel a-imino carboxylic acid derivatives such as a-imino phenyl ester, perfluoroalkyl etsers, imides, and thioester. The asymmetric Mannich reaction of those novel imine derivatives with 1,3-dicarbonyl compound is also described, and the novel a-imino imide gave improved chemical yield and stereoselectivity compared with those obtained by the use of the conventional a-imino ester-type substrate.

Preparations, X-ray crystal structure determinations, and base strength measurements of substituted tritylamines

A range of tritylamines TrNRR′, and 4-methoxy-, 4,4′-dimethoxy-, and 4,4′,4″-trimethoxy-substituted analogues, have been prepared from (substituted) trityl chloride, bromide, or tetrafluoroborate with ammonia or with amines HNRR′ where R and R′ are hydrog