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84000-04-4

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84000-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84000-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,0 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84000-04:
(7*8)+(6*4)+(5*0)+(4*0)+(3*0)+(2*0)+(1*4)=84
84 % 10 = 4
So 84000-04-4 is a valid CAS Registry Number.

84000-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 9H-fluoren-9-ylmethyl (S)-4-[(benzyloxy)methyl]-5-oxo-1,3-oxazolidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names (4S)-4-[(benzyloxy)methyl]-3-(9-fluorenylmethyloxycarbonyl)-5-oxooxazolidine

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:84000-04-4 SDS

84000-04-4Relevant articles and documents

Fluorenylmethoxycarbonyl-N-methylamino acids synthesized in a flow tube-in-tube reactor with a liquid-liquid semipermeable membrane

Buba, Annette E.,Koch, Stefan,Kunz, Horst,Loewe, Holger

supporting information, p. 4509 - 4513 (2013/07/26)

Both steps of the N-methylation of 9-fluorenylmethoxycarbonyl (Fmoc) amino acids were carried out in a microstructured tube-in-tube reactor equipped with a semipermeable Teflon AF 2400 membrane as the inner tubing. In the first step, gaseous formaldehyde

Synthesis of 9-Fluorenylmethyloxycarbonyl-Protected N-Alkyl Amino Acids by Reduction of Oxazolidinones

Freidinger, Roger M.,Hinkle, Jeffery S.,Perlow, Debra S.,Arison, Byron H.

, p. 77 - 81 (2007/10/02)

A new two-step synthesis of Fmoc-protected N-alkyl amino acids has been developed.The first step involves acid-catalyzed condensation of an Fmoc-protected amino acid with an aldehyde to form an oxazolidinone.This intermediate is then reduced with triethyl

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