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269726-95-6

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269726-95-6 Usage

General Description

Fmoc-(R)-3-Amino-5-hexenoic acid is a chemical compound used in scientific research, particularly in the field of molecular biology. It belongs to the group of Fmoc-amino acids, which are often used in solid-phase peptide synthesis (SPPS), a method of creating peptides and proteins. Fmoc-(R)-3-Amino-5-hexenoic acid is known for its stability and resistance to side reactions, making it suitable for complex peptide syntheses. Its structure contains a carboxyl group (COOH) and an amine group (NH2), giving it both acidic and basic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 269726-95-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,7,2 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 269726-95:
(8*2)+(7*6)+(6*9)+(5*7)+(4*2)+(3*6)+(2*9)+(1*5)=196
196 % 10 = 6
So 269726-95-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H21NO4/c1-2-7-14(12-20(23)24)22-21(25)26-13-19-17-10-5-3-8-15(17)16-9-4-6-11-18(16)19/h2-6,8-11,14,19H,1,7,12-13H2,(H,22,25)(H,23,24)/t14-/m1/s1

269726-95-6SDS

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 FMOC-(R)-3-AMINO-5-HEXENOIC ACID

1.2 Other means of identification

Product number -
Other names N-(9-FLUORENYLMETHOXYCARBONYL)-(R)-3-AMINO-5-HEXENOIC ACID

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:269726-95-6 SDS

269726-95-6Downstream Products

269726-95-6Relevant articles and documents

Synthesis of a natural product-inspired eight-membered ring lactam library via ring-closing metathesis

Brown, Neil,Xie, Baohan,Markina, Nataliya,VanderVelde, David,Perchellet, Jean-Pierre H.,Perchellet, Elisabeth M.,Crow, Kyle R.,Buszek, Keith R.

scheme or table, p. 4876 - 4879 (2009/05/30)

We have prepared a novel speculative eight-membered lactam demonstration library based on the skeletal structure of the potent antitumor marine natural product octalactin A. The basic scaffold was readily constructed in a convergent fashion via ring-closing metathesis chemistry from the corresponding diene amides. A cursory examination of the biological properties of the library validates the relevance and significance of these structures.

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