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tert-butyl N-[2-methyl-1-[(2S)-2-[[(2S)-1-methylpyrrolidine-2-carbonyl ]carbamoyl]pyrrolidin-1-yl]-1-oxo-propan-2-yl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84902-97-6

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84902-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84902-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84902-97:
(7*8)+(6*4)+(5*9)+(4*0)+(3*2)+(2*9)+(1*7)=156
156 % 10 = 6
So 84902-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H34N4O5/c1-19(2,3)29-18(28)22-20(4,5)17(27)24-12-8-10-14(24)16(26)21-15(25)13-9-7-11-23(13)6/h13-14H,7-12H2,1-6H3,(H,22,28)(H,21,25,26)/t13-,14-/m0/s1

84902-97-6SDS

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 tert-butyl N-[2-methyl-1-[2-[(1-methylpyrrolidine-2-carbonyl)carbamoyl]pyrrolidin-1-yl]-1-oxopropan-2-yl]carbamate

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:84902-97-6 SDS

84902-97-6Downstream Products

84902-97-6Relevant academic research and scientific papers

MULTIPLE CONFORMATIONAL STATES OF A PRO-PRO PEPTIDE. SOLID-STATE AND SOLUTION CONFORMATIONS OF BOC-AIB-PRO-PRO-NHME.

Balaram,Prasad,Balaram

, p. 4065 - 4071 (1983)

The solid-state and solution conformations of the model peptide Boc-Aib-Pro-Pro-NHMe have been studied by X-ray diffraction and NMR. The peptide adopts a poly(proline II) conformation in the solid state. Two molecules are observed in the asymmetric unit differing in the geometry (cis/trans) of the urethane group. The molecules are held together in the crystal by a complex network of hydrogen bonds involving three molecules of water, which cocrystallize. Dissolution of single crystals at low temperature permits NMR observation of the solid-state conformer. In solution, the peptide undergoes a trans-cis isomerization of the Pro-Pro bond. Low-temperature NMR measurements allow the detection of three conformational states of the Pro-Pro segment.

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