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17083-25-9

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17083-25-9 Usage

Chemical structure

consists of an amino group and a tert-butoxy group attached to a propionic acid backbone

Derivative of

alanine amino acid

Uses

commonly used in the synthesis of pharmaceuticals and agrochemicals

Solubility

relatively high level of solubility in organic solvents due to tert-butoxy group and amino group

Importance in peptide bond formation

presence of amino group crucial in the formation of peptide bonds, key process in the synthesis of proteins and other biological molecules

Check Digit Verification of cas no

The CAS Registry Mumber 17083-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,8 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17083-25:
(7*1)+(6*7)+(5*0)+(4*8)+(3*3)+(2*2)+(1*5)=99
99 % 10 = 9
So 17083-25-9 is a valid CAS Registry Number.

17083-25-9SDS

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 2-amino-3-tert-butoxypropionic acid

1.2 Other means of identification

Product number -
Other names H-Ser(t-Bu)-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:17083-25-9 SDS

17083-25-9Relevant articles and documents

DIARYLSULPHID BACKBONE CONTAINING PHOTOLABILE PROTECTING GROUPS

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Page/Page column 41-42, (2012/10/18)

The present invention relates to photoactivable protecting groups containing a diarylsulphid chromophore, a method for the synthesis thereof and their use as photoactivable protecting groups using maskless photolithography based array synthesis. wherein R2 is [Formula II] or wherein R2 is [Formula III] or [Formula IV] wherein R7 is a natural amino acid, a non-natural amino acid or an amino acid derivative forming an urethan bond to formula Ib, or wherein formula IV represents the carboxy function of a natural amino acid, a non-natural amino acid or an amino acid derivative, forming an ester bond to formula Ib.

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