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130309-33-0

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  • (R)-Nα-9-Fluorenylmethoxycarbonyl-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid

    Cas No: 130309-33-0

  • USD $ 1.2-5.0 / Kiloliter

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130309-33-0 Usage

Chemical Properties

white crystalline powder

Uses

Fmoc-D-Tic-OH, is an amino acid derivative used in peptide chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 130309-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,3,0 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130309-33:
(8*1)+(7*3)+(6*0)+(5*3)+(4*0)+(3*9)+(2*3)+(1*3)=80
80 % 10 = 0
So 130309-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C25H21NO4/c27-24(28)23-13-16-7-1-2-8-17(16)14-26(23)25(29)30-15-22-20-11-5-3-9-18(20)19-10-4-6-12-21(19)22/h1-12,22-23H,13-15H2,(H,27,28)/p-1/t23-/m1/s1

130309-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-(-)-2-(9-Fluorenylmethoxycarbonyl)-1,2,3,4-Tetrahydro-3-Isoquinolinecarboxylic Acid

1.2 Other means of identification

Product number -
Other names Fmoc-D-Tic-OH

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:130309-33-0 SDS

130309-33-0Relevant articles and documents

Solid-phase synthesis and utilization of side-chain reactive unnatural amino acids

O'Donnell, Martin J.,Alsina, Jordi,Scott, William L.

, p. 8403 - 8406 (2007/10/03)

Alkylation of the benzophenone imine of glycine Wang resin with α,ω-dihaloalkanes yielded valuable reactive intermediates. These racemic ω-chloro or ω-bromo intermediates were converted to α-amino acids containing diverse side-chain functionalities (e.g.

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