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L-Alanine, N-[(phenylmethoxy)carbonyl]-, 9H-fluoren-9-ylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85933-03-5

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85933-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85933-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,3 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85933-03:
(7*8)+(6*5)+(5*9)+(4*3)+(3*3)+(2*0)+(1*3)=155
155 % 10 = 5
So 85933-03-5 is a valid CAS Registry Number.

85933-03-5SDS

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 (S)-2-Benzyloxycarbonylamino-propionic acid 9H-fluoren-9-ylmethyl ester

1.2 Other means of identification

Product number -
Other names -

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:85933-03-5 SDS

85933-03-5Downstream Products

85933-03-5Relevant academic research and scientific papers

Preparation and Properties of Nα-Di-tert-Butoxycarbonyl Amino Acids. Applicability in the Synthesis of Leu-Enkephalin

Gunnarsson, Kerstin,Ragnarsson, Ulf

, p. 944 - 951 (2007/10/02)

The synthesis of Nα-di-tert-butoxycarbonyl amino acids starting from the corresponding mono-derivatives via a three-step route is reported.The latter were converted into a suitable ester and then exhaustively t-butoxycarbonylated, after which t

9-FLUORENYLMETHYL ESTERS AS CARBOXYL PROTECTING GROUP

Kessler, Horst,Siegmeier, Rainer

, p. 281 - 282 (2007/10/02)

The use of 9-fluorenylmethyl esters for the protection of carboxyl groups is proposed.The advantage of this group is the selective deprotection under mild conditions using secondary amines without racemization.

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