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212651-48-4

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212651-48-4 Usage

Chemical Properties

White to off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 212651-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,6,5 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 212651-48:
(8*2)+(7*1)+(6*2)+(5*6)+(4*5)+(3*1)+(2*4)+(1*8)=104
104 % 10 = 4
So 212651-48-4 is a valid CAS Registry Number.

212651-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Fmoc-Gly-Pro

1.2 Other means of identification

Product number -
Other names N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-GLYCINYL-L-PROLINE

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:212651-48-4 SDS

212651-48-4Downstream Products

212651-48-4Relevant articles and documents

Use of an internal reference for the quantitative HPLC-UV analysis of solid-phase reactions: A case study of 2-chlorotrityl chloride resin

Spengler, Jan,Fernandez-Llamazares, Anna-Iris,Albericio, Fernando

supporting information, p. 229 - 234 (2013/07/11)

Here we evaluated the use of internal reference compounds for the rapid assessment of reactions performed in solid-phase. An internal reference compound (commercially available) was bound to the resin, together with the substrate, and cleaved with the products after completion of the reaction. The peak area of the reference compound in the HPLC-UV chromatograms can be correlated directly with those of other compounds present in the reaction mixture, thereby allowing a quantitative interpretation of the chromatograms with respect to conversion and yield. The usefulness of this method was demonstrated by optimization of a protocol for the synthesis of proline-based tripeptides.

Peptide bond isosteres: Ester or (E)-alkene in the backbone of the collagen triple helix

Jenkins, Cara L.,Vasbinder, Melissa M.,Miller, Scott J.,Raines, Ronald T.

, p. 2619 - 2622 (2007/10/03)

(Chemical Equation Presented) Collagen is the most abundant protein in animals. Interstrand N-H...O=C hydrogen bonds between backbone amide groups form a ladder in the middle of the collagen triple helix. Isosteric replacement of the hydrogen-bond-donatin

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