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125760-26-1

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125760-26-1 Usage

Uses

N-(9-Fluorenylmethoxycarbonyl)-L-serine Phenacyl Ester is used in preparation of protected Serine.Also, used in preparation of Glycoside Glycosylceramide analogs as immunomodulators and antitumor agents.

Check Digit Verification of cas no

The CAS Registry Mumber 125760-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,7,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125760-26:
(8*1)+(7*2)+(6*5)+(5*7)+(4*6)+(3*0)+(2*2)+(1*6)=121
121 % 10 = 1
So 125760-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C26H23NO6/c28-14-23(25(30)32-16-24(29)17-8-2-1-3-9-17)27-26(31)33-15-22-20-12-6-4-10-18(20)19-11-5-7-13-21(19)22/h1-13,22-23,28H,14-16H2,(H,27,31)/t23-/m0/s1

125760-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(9-Fluorenylmethoxycarbonyl)-L-serine Phenacyl Ester

1.2 Other means of identification

Product number -
Other names phenacyl (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoate

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:125760-26-1 SDS

125760-26-1Downstream Products

125760-26-1Relevant articles and documents

A Stable Pyrophosphoserine Analog for Incorporation into Peptides and Proteins

Yates, Lisa M.,Fiedler, Dorothea

, p. 1066 - 1073 (2016)

Protein pyrophosphorylation is a covalent modification of proteins, mediated by the inositol pyrophosphate messengers. Although the inositol pyrophosphates have been linked to a range of cellular processes, the role of protein pyrophosphorylation remains minimally characterized in vivo. The inherent instability of the phosphoanhydride bond has hampered the development of useful bioanalytical techniques to interrogate this novel signaling mechanism. Here, we describe the preparation of a pyrophosphoserine analog containing a stable methylene-bisphosphonate group that is compatible with solid-phase peptide synthesis. The resulting peptides demonstrate enhanced stability in Eukaryotic cell lysates and mammalian plasma and display resistance toward chemical degradation, when compared to the corresponding pyrophosphopeptides. In addition, the peptides containing the stable pyrophosphoserine analog are highly compatible with common ligation methods, such as native chemical ligation, maleimide conjugation, and glutaraldehyde ligation. The bisphosphonate-containing peptides will, therefore, be well-suited for future pyrophosphoserine antibody generation and affinity capture of pyrophosphoprotein binding partners and provide a key entry point to study the regulatory role of protein pyrophosphorylation.

An Efficient Procedure for Solid Phase Synthesis of Phosphopeptides by the Fmoc Strategy

Wakamiya, Tateaki,Saruta, Kunio,Yasuoka, Jun-ichi,Kusumoto, Shoichi

, p. 1099 - 1102 (2007/10/02)

The Fmoc-mode solid-phase method was succesfully applied to establish a practical procedure for the synthesis of phosphopeptides.Both Fmoc-phosphoserine with free phosphoric moiety and its monobenzyl phosphate derivative were examined as one of starting materials for the synthesis of peptides.The employment of the latter gave better result in respects of the yield and purity of the product than that obtained with the former.

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