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13574-84-0

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13574-84-0 Usage

Chemical Properties

white amorphous powder

Check Digit Verification of cas no

The CAS Registry Mumber 13574-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,7 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13574-84:
(7*1)+(6*3)+(5*5)+(4*7)+(3*4)+(2*8)+(1*4)=110
110 % 10 = 0
So 13574-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H23NO6/c1-17(2,3)24-16(22)18-13(15(20)21)9-10-14(19)23-11-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H,18,22)(H,20,21)

13574-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyclohexylcyclohexanamine,(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-5-phenylmethoxypentanoic acid

1.2 Other means of identification

Product number -
Other names Boc-L-aspartic acid 1-amide

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:13574-84-0 SDS

13574-84-0Relevant academic research and scientific papers

NMR-Spectroscopic Assignment of the Aib-Methyl Groups in α-Helical and β-Turn Environment with the Use of Selectively Deuterated Aib. The Solution Conformations of Boc-Ala-Aib-Ala-OMe

Leibfritz, Dieter,Brunne, Roger M.,Weihrauch, Thomas,Stelten, Johannes,Haupt, Erhard T.K.,Stohrer, Wolf-Dieter

, p. 1017 - 1028 (2007/10/02)

Boc-Ala-Aib-Ala-OMe (1a) adopts in the crystal a conformation similar to a β-turn type II.From 13C-CP-MAS spectra the magnetic nonequivalence of the Aib-Cβ atoms amounts to 6.1 ppm.The pro-S-Cβ carbon signal is shifted upfield as can be shown by comparison with the spectra of Boc-Ala-(R)-Aib-Ala-OMe (1b).This assignment corresponds to a downfield shift of the Aib pro-S-Cβ carbon in the helix of Boc-4-Aib-7-O-PEG-M (2a), where it was established with the aid of the (R)-Aib-containing analog (2b).From molecular dynamics simulations of Boc-Ala-Aib-Ala-OMe we propose two major conformational species in solution that account for the observed MNE of 2.1 ppm, the temperature gradients of the amide protons, the coupling constants, and the distances derived from ROESY spectra.

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