(1E)-1-Methoxy-N-(Triethylazaniumyl)Sulfonylmethanimidate; (Methoxycarbonylsulfamoyl)Triethylammonium Hydroxide Inner Salt; (Methoxycarbonylsulfamoyl)Triethylammonium Hydroxide; Mcsta; Burgess'S Reagent; Methyl N-(Triethylammoniosulfonyl)Carbamate; Burgess Dehydration Reagent; (Methoxycarbonylsulfamoyl)Triethylammonium Hydroxide, Inner Salt

Teniposide

MSDS

CAS:29767-20-2

Molecular Formula:C32H32O13S

Alias

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Etp; Vumon; Vm-26; Pipodophyllotoxin Vm 26; Vehem; Teniposide(Vumon); Teniposide/Vm-26

Brief Introduction

It is mainly used in leukemia, malignant lymphoma, neuroblastoma, brain tumor, He Jiejin's disease, bladder cancer, small cell lung cancer and so on.

Cinnarizine

MSDS

CAS:298-57-7

Molecular Formula:C26H28N2

Alias

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1-Trans-Cinnamyl-4-Diphenylmethylpiperazine; Stugeron; Dimitronal; Stutgin; 1-Benzhydryl-4-[(E)-3-Phenylprop-2-Enyl]Piperazine

Brief Introduction

Long acting multifunctional vasoconstrictor antagonist can dilate blood vessels, improve blood circulation and prevent vascular embrittlement. It can also be used to treat cerebrovascular diseases, headache, dizziness, insomnia, memory loss, hemiplegia, limb numbness and weakness, unclear speech and other diseases caused by cervical vertigo.

(1S,2S)-1,2-Diphenylethane-1,2-Diamine

MSDS

CAS:29841-69-8

Molecular Formula:C14H16N2

Alias

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(1S,2S)-(-)-1,2-Diphenylethylenediamine; (1S,2S)-1,2-Diamino-1,2-Diphenylethane; (S,S)-1,2-Diphenyl-1,2-Ethanodiamine; (S,S)-1,2-Diphenylethylenediamine; (S,S)-1,2-Diphenyl-1,2-Diaminoethane; (1S,2S)-1,2-Diphenyl-1,2-Ethanediamine; (1S,2S)-(-)-1,2-Diphenyldiaminoethane; (1S,2S)-(-)-1,2-Diphenyl-1,2-Ethanediamine; (-)-1,2-Diphenylethylenediamine; (1S,2S)-(-)-1,2-Diamino-1,2-Diphenylethane; (1S,2S)-Dpen; (S,S)-DPEN; (1S,2S)-(-)-1,2-Diphenyl-1,2-Ethane Diamine

Brief Introduction

Widely used in asymmetric synthesis and optical resolution, such as asymmetric hydroxylation of olefins, asymmetric aldol condensation, asymmetric Diels-Alder reaction, asymmetric allylation of carbonyl groups, optically active propylene Synthesis of dienyl alcohols and propynyl alcohols, asymmetric epoxidation of olefins without functional groups, and resolution of binaphthol.

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