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161529-14-2

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161529-14-2 Usage

General Description

FMOC-(S)-3-amino-4-hydroxybutanoic acid t-butyl ester is a compound used in organic synthesis and peptide chemistry. It consists of a t-butyl ester group attached to a (S)-3-amino-4-hydroxybutanoic acid molecule, which also contains a FMOC (9-fluorenylmethoxycarbonyl) protecting group. FMOC-(S)-3-AMINO-4-HYDROXYBUTANOIC ACID T-BUTYL ESTER is commonly used in the solid-phase peptide synthesis as a building block for the assembly of peptide chains. It is also used as a chiral auxiliary in various organic reactions, and as a precursor for the synthesis of pharmaceutical compounds and biologically active peptides.

Check Digit Verification of cas no

The CAS Registry Mumber 161529-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,5,2 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 161529-14:
(8*1)+(7*6)+(6*1)+(5*5)+(4*2)+(3*9)+(2*1)+(1*4)=122
122 % 10 = 2
So 161529-14-2 is a valid CAS Registry Number.

161529-14-2SDS

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 9H-fluoren-9-ylmethyl N-[(2S)-1-hydroxy-4-oxo-4-(tritylamino)butan-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names AmbotzFAL3050

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:161529-14-2 SDS

161529-14-2Relevant articles and documents

PEPTIDE-OLIGOUREA HYBRID COMPOUNDS

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Paragraph 00287-00289, (2020/07/31)

The present description relates to peptidomimetic foldamers, and their synthesis. In particular, the description provides peptide-amino urea hybrid peptidomimetic foldamers comprising an alpha amino acid peptide portion and an oligourea portion.

Process for preparing sulfonamide compounds

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Paragraph 0415; 0453-0456; 0494; 0579-0582, (2020/07/24)

The invention relates to a process for preparing sulfonamide compounds. The sulfonamide compound is an inhibitor of Bcl-2/Bcl-xL and is prepared from a compound (3R)-1-(3-(4-(4-(4-(3-(2-(4-chlorphenyl)-1-isopropyl-4-methylsulfonyl-5-methyl-1H-pyrrole-3-yl

iSPAAC: Isomer-Free Generation of a Bcl-xL-Inhibitor in Living Cells

Lis, Christian,Rubner, Stefan,Gr?st, Corinna,Hoffmann, Ralf,Knappe, Daniel,Berg, Thorsten

supporting information, p. 13762 - 13766 (2018/09/14)

Strain-promoted azide–alkyne cycloadditions (SPAAC) have proven extremely useful for labeling of biomolecules, but typically produce isomeric mixtures. This is not appropriate for the formation of bioactive molecules in living cells. Here, the first use o

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