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120081-14-3

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  • (2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-acetamido-3-hydroxypropanoyl]amino]-4-hydroxy-4-oxobutanoyl]amino]-6-aminohexanoyl]pyrrolidine-2-carboxylicacid

    Cas No: 120081-14-3

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120081-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120081-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,0,8 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120081-14:
(8*1)+(7*2)+(6*0)+(5*0)+(4*8)+(3*1)+(2*1)+(1*4)=63
63 % 10 = 3
So 120081-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H33N5O9/c1-11(27)22-14(10-26)18(31)24-13(9-16(28)29)17(30)23-12(5-2-3-7-21)19(32)25-8-4-6-15(25)20(33)34/h12-15,26H,2-10,21H2,1H3,(H,22,27)(H,23,30)(H,24,31)(H,28,29)(H,33,34)/t12-,13-,14-,15-/m0/s1

120081-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-acetamido-3-hydroxypropanoyl]amino]-3-carboxypropanoyl]amino]-6-aminohexanoyl]pyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names N-acetyl-Ser-Asp-Lys-Pro

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:120081-14-3 SDS

120081-14-3Downstream Products

120081-14-3Relevant articles and documents

Rapid, continuous solution-phase peptide synthesis: Application to peptides of pharmaceutical interest

Carpino, Louis A.,Ghassemi, Shahnaz,Ionescu, Dumitru,Ismail, Mohamed,Sadat-Aalaee, Dean,Truran, George A.,Mansour,Siwruk, Gary A.,Eynon, John S.,Morgan, Barry

, p. 28 - 37 (2003)

The Fmoc/TAEA and Bsmoc/TAEA methods for the rapid, continuous solution synthesis of peptide segments are shown to be applicable to the gram-scale synthesis of short peptides as well as, for the first time, to the synthesis of a relatively long (22-mer) segment, (hPTH 13-34). In the latter case the crude product was of significantly greater purity than a sample obtained via a solid-phase protocol. The Bsmoc methodology was optimized by a new technique involving filtration of the growing partially deprotected peptide at each coupling-deprotection cycle through a short column of silica gel.

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