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111061-56-4

111061-56-4

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111061-56-4 Usage

Chemical Properties

white to light yellow crystal powde

Check Digit Verification of cas no

The CAS Registry Mumber 111061-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,6 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 111061-56:
(8*1)+(7*1)+(6*1)+(5*0)+(4*6)+(3*1)+(2*5)+(1*6)=64
64 % 10 = 4
So 111061-56-4 is a valid CAS Registry Number.
InChI:InChI=1/C37H31NO5/c39-35(40)34(38-36(41)42-24-33-31-22-12-10-20-29(31)30-21-11-13-23-32(30)33)25-43-37(26-14-4-1-5-15-26,27-16-6-2-7-17-27)28-18-8-3-9-19-28/h1-23,33-34H,24-25H2,(H,38,41)(H,39,40)/t34-/m1/s1

111061-56-4 Well-known Company Product Price

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  • Aldrich

  • (47563)  Fmoc-Ser(Trt)-OH  ≥98.0%

  • 111061-56-4

  • 47563-5G-F

  • 1,337.31CNY

  • Detail

111061-56-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-trityloxypropanoic acid

1.2 Other means of identification

Product number -
Other names N-Fmoc-L-Ser-(Trt)-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:111061-56-4 SDS

111061-56-4Relevant articles and documents

Application of the Trt and Fmoc Groups for the Protection of Polyfunctional α-Amino Acids

Barlos, Kleomenis,Mamos, Petros,Papaioannou, Dionysios,Patrianakou, Stella,Sanida, Chariklia,Schaefer, Wolfram

, p. 1025 - 1030 (2007/10/02)

Simple methods for the preparation of ditrityl amino acids 3 and their application for the synthesis of the peptides 9-27 are described.Selective detritylation of 3 and of the synthesized ditrityl peptides is achieved with 1percent trifluoroacetic acid in dichloromethane.The resulting Nα-detritylated amino acids 5 were converted into the corresponding fluorenylmethoxycarbonyl amino acids 6 under Schotten-Baumann conditions using fluorenylmethyl chloroformate.

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