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55260-24-7

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55260-24-7 Usage

Chemical Properties

White powder

Uses

Boc-Gln(Xan)-OH, is an amino acid derivative used in chemical synthesis and peptide chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 55260-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,6 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55260-24:
(7*5)+(6*5)+(5*2)+(4*6)+(3*0)+(2*2)+(1*4)=107
107 % 10 = 7
So 55260-24-7 is a valid CAS Registry Number.
InChI:InChI=1/C23H26N2O6/c1-23(2,3)31-22(29)24-16(21(27)28)12-13-19(26)25-20-14-8-4-6-10-17(14)30-18-11-7-5-9-15(18)20/h4-11,16,20H,12-13H2,1-3H3,(H,24,29)(H,25,26)(H,27,28)/t16-/m0/s1

55260-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-5-(9H-xanthen-9-ylamino)pentanoic acid

1.2 Other means of identification

Product number -
Other names BOC-Nd-XANTHYL-L-GLUTAMINE

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:55260-24-7 SDS

55260-24-7Relevant articles and documents

Peptide Synthesis. Part 3. Comparative Solid-phase Syntheses of Human β-Endorphin on Polyamide Supports using t-Butoxycarbonyl and Fluorenylmethoxycarbonyl Protecting Groups

Atherton, Eric,Caviezel, Mario,Fox, Hazel,Harkiss, Diana,Over, Hilary,Sheppard, Robert C.

, p. 65 - 73 (2007/10/02)

Solid-phase syntheses of the 31 residue peptide human β-endorphin on polar polyamide supports are described.Minimisation of acidic reaction conditions by replacement of the customary t-butoxycarbonyl and benzyl-based protecting groups by fluorenylmethoxyc

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