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105229-14-9

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105229-14-9 Usage

General Description

The chemical "1,3-Benzodioxole-5-propanoicacid,a-amino-b-hydroxy-,[S-(R*,S*)]-" is a compound with a long and complex name. It is a chiral molecule, meaning it has a non-superimposable mirror image. 1,3-Benzodioxole-5-propanoicacid,a-amino-b-hydroxy-,[S-(R*,S*)]- contains a benzodioxole ring structure and is composed of both an amino and hydroxy group, along with a propanoic acid moiety. The stereochemistry of the compound is designated as (S-(R*,S*)). 1,3-Benzodioxole-5-propanoicacid,a-amino-b-hydroxy-,[S-(R*,S*)]- may have potential applications in pharmaceuticals, as chiral molecules are often used in drug development due to their unique biological activities. Further research and analysis would be needed to determine the specific properties and potential uses of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 105229-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,2 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 105229-14:
(8*1)+(7*0)+(6*5)+(5*2)+(4*2)+(3*9)+(2*1)+(1*4)=89
89 % 10 = 9
So 105229-14-9 is a valid CAS Registry Number.

105229-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3S)-2-amino-3-(1,3-benzodioxol-5-yl)-3-hydroxypropanoic acid

1.2 Other means of identification

Product number -
Other names (2R,3S)-2-Amino-3-(benzo[d][1,3]dioxol-5-yl)-3-hydroxypropanoic 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:105229-14-9 SDS

105229-14-9Downstream Products

105229-14-9Relevant articles and documents

Synthesis of β-hydroxy-α-amino acids with a reengineered alanine racemase

Fesko, Kateryna,Giger, Lars,Hilvert, Donald

supporting information; experimental part, p. 5987 - 5990 (2009/06/25)

The Y265A mutant of alanine racemase (alrY265A) was evaluated as a catalyst for the synthesis of β-hydroxy-α-amino acids. It promotes the PLP-dependent aldol condensation of glycine with a range of aromatic aldehydes. The desired products were obtained wi

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