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CAS

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1001067-11-3

(R)-N-(9-fluorenylmethoxycarbonyl)-1-phenylethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1001067-11-3 Structure

  • Basic information

    1. Product Name: (R)-N-(9-fluorenylmethoxycarbonyl)-1-phenylethanamine
    2. Synonyms: (R)-N-(9-fluorenylmethoxycarbonyl)-1-phenylethanamine
    3. CAS NO:1001067-11-3
    4. Molecular Formula:
    5. Molecular Weight: 343.425
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1001067-11-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-N-(9-fluorenylmethoxycarbonyl)-1-phenylethanamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-N-(9-fluorenylmethoxycarbonyl)-1-phenylethanamine(1001067-11-3)
    11. EPA Substance Registry System: (R)-N-(9-fluorenylmethoxycarbonyl)-1-phenylethanamine(1001067-11-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1001067-11-3(Hazardous Substances Data)

1001067-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1001067-11-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,0,6 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1001067-11:
(9*1)+(8*0)+(7*0)+(6*1)+(5*0)+(4*6)+(3*7)+(2*1)+(1*1)=63
63 % 10 = 3
So 1001067-11-3 is a valid CAS Registry Number.

1001067-11-3Downstream Products

1001067-11-3Relevant articles and documents

An efficient and expeditious Fmoc protection of amines and amino acids in aqueous media

Gawande, Manoj B.,Branco, Paula S.

supporting information; experimental part, p. 3355 - 3359 (2012/01/06)

A new and environmentally friendly Fmoc protection of a variety of aliphatic and aromatic amines, amino acids, amino alcohols and amino phenols is reported in aqueous media under mild and catalyst-free conditions. The reaction proved to be chemoselective in presence of ambident nucleophiles.

Development of column-free alkoxycarbonyl, aryloxycarbonyl, and acyl transfer reagents

Shimizu, Mamoru,Sodeoka, Mikiko

experimental part, p. 1301 - 1312 (2009/07/05)

Easy-to-handle alkoxycarbonyl, aryloxycarbonyl, and acyl transfer reagents, which contain 3-nitro-1,2,4-triazole (NT) as a leaving group, were developed. With these reagents (NT reagents), which are stable nonhygroscopic crystalline materials, the reactions can be accomplished in about 5 min, and product can be isolated without tedious column chromatographic purification.

Convenient method for the preparation of carbamates, carbonates, and thiocarbonates

Shimizu, Mamoru,Sodeoka, Mikiko

, p. 5231 - 5234 (2008/09/17)

(Chemical Equation Presented) A convenient, rapid, and efficient method for the preparation of carbamates from amines with 1-alkoxycarbonyl-3-nitro-1,2,4- triazole transfer reagents is reported. Reactions of newly synthesized stable crystalline reagents with alkyl amines were completed in a few minutes without any additional base, and highly pure carbamates were obtained without chromatographic purification. These highly active reagents are also useful for the selective protection of nucleobases and preparation of carbonates and thiocarbonates.

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