Cas no 84418-43-9 (Fmoc-nh2)

Fmoc-nh2 structure
Fmoc-nh2 structure
Product Name:Fmoc-nh2
CAS No:84418-43-9
MF:C15H13NO2
MW:239.269223928452
MDL:MFCD00237376
CID:60696
PubChem ID:87560931
Update Time:2024-10-26

Fmoc-nh2 Chemical and Physical Properties

Names and Identifiers

    • 9-Fluorenylmethyl carbamate
    • Fmoc-amide
    • 9H-fluoren-9-ylmethyl carbamate
    • FMOC-NH2
    • Fmoc-NH2 (9-Fluorenylmethyl carbamate)
    • Carbamic Acid 9-Fluorenylmethyl Ester
    • (9H-Fluoren-9-ylmethoxy)carboxamide
    • 9-Fluorenylmethylcarbamate
    • (9h-fluoren-9-yl)methyl carbamate
    • Fmoc amine
    • FMOC-amine
    • N-(9-Fluorenylmethoxycarbonyl)amide
    • PubChem12066
    • fluoren-9-ylmethyl aminooate
    • KSC448A6B
    • ZZOKVYOCRSMTSS-UHFFFAOYSA-N
    • EBD54105
    • AN
    • 9H-Fluorene-9-methanol, carbamate (9CI)
    • 9-Fluorenylmethoxycarbonylamine
    • DB-029405
    • CS-W016703
    • AC1112
    • 9-Fluorenyl-methyl-carbamate
    • SCHEMBL113270
    • M02862
    • VP1
    • AKOS015907601
    • AS-17607
    • 9-Fluorenylmethyl carbamate, >=99.0% (HPLC)
    • MFCD00237376
    • J-519510
    • SCHEMBL2192202
    • 84418-43-9
    • DTXSID00352990
    • F0689
    • SY019088
    • Fmoc-nh2
    • MDL: MFCD00237376
    • Inchi: 1S/C15H13NO2/c16-15(17)18-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2,(H2,16,17)
    • InChI Key: ZZOKVYOCRSMTSS-UHFFFAOYSA-N
    • SMILES: O=C(N)OCC1C2C(=CC=CC=2)C2C1=CC=CC=2

Computed Properties

  • Exact Mass: 239.09500
  • Monoisotopic Mass: 239.095
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 3
  • Complexity: 296
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 52.3
  • XLogP3: 2.7

Experimental Properties

  • Density: 1.2390
  • Melting Point: 201-204?°C
  • Boiling Point: 459.7℃ at 760 mmHg
  • Flash Point: 242.3°C
  • Refractive Index: 1.627
  • Solubility: dioxane: 15?mg/mL, clear, colorless
  • PSA: 52.32000
  • LogP: 3.59450

Fmoc-nh2 Security Information

Fmoc-nh2 Customs Data

  • HS CODE:2924299090
  • Customs Data:

    China Customs Code:

    2924299090

    Overview:

    2924299090. Other cyclic amides(Including cyclic carbamates)(Including their derivatives as well as their salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, packing

    Summary:

    2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Fmoc-nh2 Pricemore >>

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Fmoc-nh2 Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Ammonium hydroxide Solvents: Dichloromethane ;  0 °C; 0 °C → rt
Reference
Utility of 2-Diphenylphosphoryloxy-1,3-Dienes in Multicomponent Hetero-Diels-Alder Reactions to Construct Functionalized Six-Membered Nitrogen Heterocycles
He, Qiuyu; et al, Chemistry - A European Journal, 2022, 28(42),

Production Method 2

Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Acetic acid ,  Water
2.1 Reagents: Sodium hydroxide Solvents: 1,4-Dioxane ,  Water
2.2 Reagents: Hydrochloric acid Solvents: 1,4-Dioxane ,  Water
Reference
Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions
Albericio, Fernando; et al, Journal of Organic Chemistry, 1990, 55(12), 3730-43

Production Method 3

Reaction Conditions
1.1 Reagents: Potassium tert-butoxide Solvents: Dimethylformamide
1.2 Solvents: Dimethylformamide
2.1 Reagents: Hydroxyamine hydrochloride Solvents: Pyridine ,  Water
3.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Acetic acid ,  Water
4.1 Reagents: Sodium hydroxide Solvents: 1,4-Dioxane ,  Water
4.2 Reagents: Hydrochloric acid Solvents: 1,4-Dioxane ,  Water
Reference
Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions
Albericio, Fernando; et al, Journal of Organic Chemistry, 1990, 55(12), 3730-43

Production Method 4

Reaction Conditions
Reference
Facile SPS of peptides having C-terminal Asn and Gln
Breipohl, Gerhard; et al, International Journal of Peptide & Protein Research, 1990, 35(3), 281-3

Production Method 5

Reaction Conditions
1.1 Solvents: Dichloromethane ;  0 °C; 0 °C → rt; overnight, rt
Reference
Silver-catalyzed intermolecular amination of C-H groups
Li, Zigang; et al, Angewandte Chemie, 2007, 46(27), 5184-5186

Production Method 6

Reaction Conditions
1.1 Reagents: Sodium hydroxide Solvents: 1,4-Dioxane ,  Water
1.2 Reagents: Hydrochloric acid Solvents: 1,4-Dioxane ,  Water
Reference
Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions
Albericio, Fernando; et al, Journal of Organic Chemistry, 1990, 55(12), 3730-43

Production Method 7

Reaction Conditions
1.1 Reagents: Hydroxyamine hydrochloride Solvents: Pyridine ,  Water
2.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Acetic acid ,  Water
3.1 Reagents: Sodium hydroxide Solvents: 1,4-Dioxane ,  Water
3.2 Reagents: Hydrochloric acid Solvents: 1,4-Dioxane ,  Water
Reference
Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions
Albericio, Fernando; et al, Journal of Organic Chemistry, 1990, 55(12), 3730-43

Production Method 8

Reaction Conditions
1.1 Reagents: Phosphorus oxychloride
2.1 Reagents: Potassium tert-butoxide Solvents: Dimethylformamide
2.2 Solvents: Dimethylformamide
3.1 Reagents: Hydroxyamine hydrochloride Solvents: Pyridine ,  Water
4.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Acetic acid ,  Water
5.1 Reagents: Sodium hydroxide Solvents: 1,4-Dioxane ,  Water
5.2 Reagents: Hydrochloric acid Solvents: 1,4-Dioxane ,  Water
Reference
Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions
Albericio, Fernando; et al, Journal of Organic Chemistry, 1990, 55(12), 3730-43

Fmoc-nh2 Raw materials

Fmoc-nh2 Preparation Products

Fmoc-nh2 Suppliers

Suzhou Senfeida Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
(CAS:84418-43-9)9-Fluorenylmethyl carbamate
Order Number:1631813
Stock Status:in Stock
Quantity:Company Customization
Purity:98%
Pricing Information Last Updated:Monday, 14 April 2025 21:49
Price ($):discuss personally
Tiancheng Chemical (Jiangsu) Co., Ltd
Gold Member
Audited Supplier Audited Supplier
(CAS:84418-43-9)芴甲氧羰酰胺
Order Number:LE1631813
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:29
Price ($):discuss personally
Recommended suppliers
Suzhou Senfeida Chemical Co., Ltd
(CAS:84418-43-9)9-Fluorenylmethyl carbamate
1631813
Purity:98%
Quantity:Company Customization
Price ($):Inquiry
Email
Tiancheng Chemical (Jiangsu) Co., Ltd
(CAS:84418-43-9)芴甲氧羰酰胺
LE1631813
Purity:99%
Quantity:25KG,200KG,1000KG
Price ($):Inquiry
Email