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CAS

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917098-99-8

FMOC-3-ENDO-AMINOBICYCLO[2.2.1]HEPTANE-2-ENDO-CARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 917098-99-8 Structure

  • Basic information

    1. Product Name: FMOC-3-ENDO-AMINOBICYCLO[2.2.1]HEPTANE-2-ENDO-CARBOXYLIC ACID
    2. Synonyms: FMOC-3-ENDO-AMINOBICYCLO[2.2.1]HEPTANE-2-ENDO-CARBOXYLIC ACID;3-(ENDO-9-FLUORENYLMETHOXYCARBONYLAMINO)BICYCLO[2.2.1]HEPTANE-2-ENDO-CARBOXYLIC ACID
    3. CAS NO:917098-99-8
    4. Molecular Formula: C23H23NO4
    5. Molecular Weight: 377.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 917098-99-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 605.2°C at 760 mmHg
    3. Flash Point: 319.8°C
    4. Appearance: /
    5. Density: 1.34g/cm3
    6. Vapor Pressure: 1.7E-15mmHg at 25°C
    7. Refractive Index: 1.658
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: FMOC-3-ENDO-AMINOBICYCLO[2.2.1]HEPTANE-2-ENDO-CARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: FMOC-3-ENDO-AMINOBICYCLO[2.2.1]HEPTANE-2-ENDO-CARBOXYLIC ACID(917098-99-8)
    12. EPA Substance Registry System: FMOC-3-ENDO-AMINOBICYCLO[2.2.1]HEPTANE-2-ENDO-CARBOXYLIC ACID(917098-99-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 917098-99-8(Hazardous Substances Data)

917098-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 917098-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,0,9 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 917098-99:
(8*9)+(7*1)+(6*7)+(5*0)+(4*9)+(3*8)+(2*9)+(1*9)=208
208 % 10 = 8
So 917098-99-8 is a valid CAS Registry Number.
InChI:InChI=1/C23H23NO4/c25-22(26)20-13-9-10-14(11-13)21(20)24-23(27)28-12-19-17-7-3-1-5-15(17)16-6-2-4-8-18(16)19/h1-8,13-14,19-21H,9-12H2,(H,24,27)(H,25,26)/t13-,14+,20-,21+/m0/s1

917098-99-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S,3R,4S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)bicyclo[2.2.1]heptane-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-(endo-9-Fluorenylmethoxycarbonylamino)bicyclo[2.2.1]heptane-2-endo-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:917098-99-8 SDS

917098-99-8Downstream Products

917098-99-8Relevant articles and documents

Solid-phase synthesis of 6,7-cycloalkane-fused 1,4-diazepane-2,5-diones via a cyclization/release strategy

Caroen, Jurgen,Clemmen, An,Kámán, Judit,Backaert, Fréderique,Goeman, Jan L.,Fül?p, Ferenc,Van Der Eycken, Johan

, p. 148 - 160 (2015/12/23)

A solid-phase synthesis procedure for the parallel preparation of 6,7-cycloalkane-fused 1,4-diazepane-2,5-diones is described. The methodology applies α- and alicyclic β-amino acid building blocks to construct the seven-membered heterocyclic core, while a

Large-scale syntheses of FMOC-protected non-proteogenic amino acids: Useful building blocks for combinatorial libraries

Dener, Jeffrey M.,Fantauzzi, Pascal P.,Kshirsagar, Tushar A.,Kelly, Daphne E.,Wolfe, Aaron B.

, p. 445 - 449 (2013/09/07)

Convenient and reliable large-scale procedures for the protection of various amino acids with N-(9-fluorenylmethoxycarbonyl)oxysuccinimide (FMOC-OSu) are described. Commercially available 4-aminomethylbenzoic acid and trans-4-(aminomethyl)cyclohexanecarbo

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