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128917-74-8

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128917-74-8 Usage

Description

Fmoc-12-aminododecanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.

Chemical Properties

White to off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 128917-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,1 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128917-74:
(8*1)+(7*2)+(6*8)+(5*9)+(4*1)+(3*7)+(2*7)+(1*4)=158
158 % 10 = 8
So 128917-74-8 is a valid CAS Registry Number.

128917-74-8 Well-known Company Product Price

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  • Sigma-Aldrich

  • (09779)  Fmoc-12-Ado-OH  ≥98.0% (TLC)

  • 128917-74-8

  • 09779-500MG

  • 1,395.81CNY

  • Detail

128917-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 12-(9H-fluoren-9-ylmethoxycarbonylamino)dodecanoic acid

1.2 Other means of identification

Product number -
Other names Fmoc-12-Ado-OH

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:128917-74-8 SDS

128917-74-8Relevant articles and documents

Direct interaction, instrumental for signaling processes, between LacCer and Lyn in the lipid rafts of neutrophil-like cells

Chiricozzi, Elena,Ciampa, Maria Grazia,Brasile, Giuseppina,Compostella, Federica,Prinetti, Alessandro,Nakayama, Hitoshi,Ekyalongo, Roudy C.,Iwabuchi, Kazuhisa,Sonnino, Sandro,Mauri, Laura

, p. 129 - 141 (2015)

Lactosylceramide [LacCer; β-Gal-(1-4)-β-Glc-(1-1)-Cer] has been shown to contain very long fatty acids that specifically modulate neutrophil properties. The interactions between LacCer and proteins and their role in cell signaling processes were assessed

Missing Selectivity of Targeted 4β-Phorbol Prodrugs Expected to be Potential Chemotherapeutics

Tarvainen, Ilari,Zimmermann, Tomá?,Heinonen, Pia,J?ntti, Maria Helena,Yli-Kauhaluoma, Jari,Talman, Virpi,Franzyk, Henrik,Tuominen, Raimo K.,Christensen, S?ren Br?gger

, p. 671 - 677 (2020)

Targeting cytotoxic 4β-phorbol esters toward cancer tissue was attempted by conjugating a 4β-pborbol derivative with substrates for the proteases prostate-specific antigen (PSA) and prostate-specific membrane antigen (PSMA) expressed in cancer tissue. The

A Light-up 1D supramolecular nanoprobe for silver ions based on assembly of pyrene-labeled peptide amphiphiles: Cell-imaging and antimicrobial activity

Kim, Inhye,Jeong, Heon-Ho,Kim, Yong-Jae,Lee, Na-Eun,Huh, Kang-Moo,Lee, Chang-Soo,Kim, Geon Hee,Lee, Eunji

, p. 6478 - 6486 (2014)

We prepared pyrene-labeled peptide amphiphiles (PAs) consisting of a hydrophobic linear- or branched-alkyl chain (for 1 or 2, respectively) and a hydrophilic histidine-rich peptide of HGGGHGHGGGHG (HG12). Both peptides have a strong tendency to form nanofibrils (NFs) in aqueous media. The resulting histidine-coated NFs show a great binding affinity to Cu2+ as a fluorescence light-off sensor. Interestingly, the emission spectra of the pyrene probe show that the different supramolecular assemblies between 1 and 2 can significantly affect the binding affinity to specific metal ions. In particular, light-up fluorescent Ag+ detection of NFs of 2 through inhibition of photoinduced electron transfer (PET) was observed even at a low concentration of PA solution. As a means to determine the biological responsibility of 2 to Ag+, intracellular detection using the turn-on response was performed. A considerable enhancement of fluorescence in NF-loaded HeLa cells was observed. In addition, the NFs were used as a template scaffold for the production of Ag nanoparticles (AgNPs) with high monodispersity and stability. The NFs decorated with AgNPs are shown to possess highly effective and long-term antibacterial activity against both Gram-negative and -positive bacteria.

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