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Fmoc-hydrazide HCl

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Fmoc-hydrazide HCl manufacturers

  • FMOC-HYDRAZIDE HCL
  • FMOC-HYDRAZIDE HCL pictures
  • 2025-04-04
  • CAS:35661-51-9
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 1ton
Fmoc-hydrazide HCl Basic information
Product Name:Fmoc-hydrazide HCl
Synonyms:FMOC-NHNH2 HCL;N-9-FLUORENYLMETHOXYCARBONYL-CARBAZATE HYDROCHLORIDE;N-(9-FLUORENYLMETHOXYCARBONYL)-HYDRAZIDE HYDROCHLORIDE;N-(9-Fluorenylmethoxycarbonyl) hydrazine (FMOC hydrazine);Fmoc-hydrazide 9-Fluorenylmethyl carbazate;9-FluorenylMethyl carbazate, derivatization grade;9-Fluorenylmethyl carbazate, 98%, derivatization grade;9-Fluorenylmethyl carbazate, >=99%
CAS:35661-51-9
MF:C15H14N2O2
MW:254.28
EINECS:624-360-9
Product Categories:
Mol File:35661-51-9.mol
Fmoc-hydrazide HCl Structure
Fmoc-hydrazide HCl Chemical Properties
Melting point ~170 °C (dec.)
Boiling point 485.8±14.0 °C(Predicted)
density 1.259±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
pka10.21±0.20(Predicted)
form powder to crystal
color White to Almost white
BRN 2470262
InChIInChI=1S/C15H14N2O2/c16-17-15(18)19-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9,16H2,(H,17,18)
InChIKeyYGCGPEUVGHDMLO-UHFFFAOYSA-N
SMILESN(C(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O)N
CAS DataBase Reference35661-51-9
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-38-37-36
Safety Statements 26-36
WGK Germany 3
3-10
HS Code 29280000
MSDS Information
Fmoc-hydrazide HCl Usage And Synthesis
Chemical Propertieswhite powder
Uses9-Fluorenylmethyl Carbazate is a reagent for the sensitive fluorogenic derivatization of carbohydrates.
Synthesis
9-Fluorenylmethyl chloroformate

28920-43-6

FMOC-HYDRAZIDE HCL

35661-51-9

General procedure for the synthesis of 9-fluorenylmethylhydrazinyl formate from 9-fluorenylmethylhydrazinyl formate as chloroformic acid methyl ester (FmocCl): to a well-stirred solution of hydrazine hydrate (19 g, 386 mmol) dissolved in 150 mL of CH3CN/H2O (1:1, v/v) at 0 °C, FmocCl (10 g, 38.65 mmol) dissolved in a solution of 600 mL of CH3CN. The reaction mixture was then warmed to room temperature and stirring was continued for 12 hours. Upon completion of the reaction, the mixture was concentrated in vacuum to about 150 mL and filtered to give the white solid product 9-fluorenylmethylhydrazinyl formate. The product was washed sequentially with water and hexane, dried to constant weight, and finally obtained under vacuum as 9.74 g (99% yield) of a pure product with a melting point of 172-173 °C. The structure of the product was confirmed by 1H NMR and 13C NMR: 1H NMR (DMSO) δ 4.08 (brs, 2H), 4.21 (t, J = 7.2 Hz, 1H), 4.28 (d, J = 7.2 Hz, 2H), 7.32 (t, J = 7.4 Hz, 2H), 7.42 (t, J = 7.4 Hz, 2H), 7.69 ( d, J = 7.4 Hz, 2H), 7.89 (d, J = 7.4 Hz, 2H), 8.36 (brs, 1H); 13C NMR (DMSO) δ 47.7, 66.7, 121.1 (2C), 126.3 (2C), 128.1 (2C), 128.7 (2C), 141.7 (2C), 144.9 (2C), 159.2. 159.2.

References[1] Journal of Organic Chemistry, 2012, vol. 77, # 12, p. 5271 - 5278
[2] Patent: US9115171, 2015, B2. Location in patent: Page/Page column 43
[3] Patent: EP2182974, 2015, B1. Location in patent: Paragraph 0093
[4] Patent: CN108178739, 2018, A. Location in patent: Paragraph 0032; 0033; 0034
[5] Tetrahedron, 2011, vol. 67, # 42, p. 8187 - 8194
Fmoc-hydrazide HCl Preparation Products And Raw materials
Raw materials9-Fluorenylmethyl chloroformate-->Hydrazine hydrate-->Acetonitrile
Tag:Fmoc-hydrazide HCl(35661-51-9) Related Product Information
Hydrazine dihydrochloride Acethydrazide Methyl carbazate Formylhydrazine Methyl 4-amino-2-methoxybenzoate Ethyl 3-indoleacetate Hydrazine acetate Methylhydrazine 4-(FMOC-HYDRAZINO)-BENZOIC ACID FMOC-HYDRAZIDE HCL 6-FMOC-HYDRAZINONICOTINIC ACID 4-FMOC-HYDRAZINOBENZOYL AM NOVAGEL(TM) 2-N-(TERT-BUTOXYCARBONYL)-AMINO-3-(2-N-FMOC-AMINO-PYRROLIDINYL)PROPIONIC ACID RARECHEM GF HN 0001 AKOS 91273 SUCCINIMIDYL 6-FMOC-HYDRAZINONICOTINATE RARECHEM GF HN 0003 FMOC-1-AMINO-4-(2-HYDROXYETHYL)PIPERAZINE