(S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate

CAS No.：925706-40-7

Important Notice

This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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(S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate Basic information

Product Name:	(S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate
Synonyms:	(S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate;(5S)-5-benzyl-6,6-dimethyl-2-(2,4,6-trimethylphenyl)-5,8-dihydro-[1,2,4]triazolo[3,4-c][1,4]oxazin-4-ium
CAS:	925706-40-7
MF:	C23H28BF4N3O
MW:	449.2925328
EINECS:
Product Categories:
Mol File:	925706-40-7.mol

(S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate Chemical Properties

Melting point	200-206°C
storage temp.	under inert gas (nitrogen or Argon) at 2-8°C

Safety Information

WGK Germany

MSDS Information

(S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate Usage And Synthesis

Uses

Catalyst for:

Intermolecular conjugate addition of alcohols to unsaturated ketones and esters
Preparation of β-amino carbonyl compounds by N-heterocyclic carbene-catalyzed enantioselective Mannich reactions of a-aryloxyacetaldehydes with imines
Asymmetric synthesis of cyclopentenes from allyl diketones by carbene-catalyzed intramolecular aldol reaction, lactonization, and carbon dioxide expulsion
Preparation of esters via tandem oxidation of allylic/benzylic/propargyl alcohols or aldehyde

(S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate Preparation Products And Raw materials

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