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183388-64-9

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  • (2S,3S,5S)-5-tert-Butyloxycarbonylamino-2-amino-3-hydroxy-1,6-diphenylhexane succinate Manufacturer/High quality/Best price/In stock

    Cas No: 183388-64-9

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  • (2S,3S,5S)-5-tert-Butyloxycarbonylamino-2-amino-3-hydroxy-1,6-diphenylhexane succinate

    Cas No: 183388-64-9

  • USD $ 1.2-5.0 / Kiloliter

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183388-64-9 Usage

Description

(2S,3S,5S)-5-tert-Butyloxycarbonylamino-2-amino-3-hydroxy-1,6-diphenylhexane succinate is a complex chemical compound that features a succinate group attached to a 1,6-diphenylhexane backbone. (2S,3S,5S)-5-tert-Butyloxycarbonylamino-2-amino-3-hydroxy-1,6-diphenylhexane succinate is a derivative of the amino acid valine, with a tert-butyloxycarbonylamino group at the 5th carbon, and includes an amino and hydroxy group. Its unique structure and potential biological activity suggest it may have applications in the pharmaceutical industry, particularly in drug development. Further research is required to explore its properties and uses.

Uses

Used in Pharmaceutical Industry:
(2S,3S,5S)-5-tert-Butyloxycarbonylamino-2-amino-3-hydroxy-1,6-diphenylhexane succinate is used as a potential candidate for drug development due to its unique molecular structure and the possibility of exhibiting biological activity that could be harnessed for therapeutic purposes.
Further applications may be discovered as research progresses, but currently, the primary focus is on its potential within the pharmaceutical sector for creating new drugs that could address various health conditions. (2S,3S,5S)-5-tert-Butyloxycarbonylamino-2-amino-3-hydroxy-1,6-diphenylhexane succinate's specific uses will depend on the results of ongoing studies and its demonstrated efficacy and safety in preclinical and clinical trials.

Check Digit Verification of cas no

The CAS Registry Mumber 183388-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,3,8 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183388-64:
(8*1)+(7*8)+(6*3)+(5*3)+(4*8)+(3*8)+(2*6)+(1*4)=169
169 % 10 = 9
So 183388-64-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H32N2O3.C4H6O4/c1-23(2,3)28-22(27)25-19(14-17-10-6-4-7-11-17)16-21(26)20(24)15-18-12-8-5-9-13-18;5-3(6)1-2-4(7)8/h4-13,19-21,26H,14-16,24H2,1-3H3,(H,25,27);1-2H2,(H,5,6)(H,7,8)/t19-,20-,21-;/m0./s1

183388-64-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,5S)-5-tert-Butyloxycarbonylamino-2-amino-3-hydroxy-1,6-diphenylhexane succinate

1.2 Other means of identification

Product number -
Other names bdh succinate salt

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:183388-64-9 SDS

183388-64-9Relevant articles and documents

Diastereoselective synthesis of a core fragment of ritonavir and lopinavir

Roy, Arnab,Reddy, Lekkala Amarnath,Dwivedi, Namrata,Naram, Jyothirmayi,Swapna, Rodda,Malakondaiah, Golla China,Ravikumar, Mylavarpu,Bhalerao, Dinesh,Pratap, Taduri Bhanu,Reddy, Padi Pratap,Bhattacharya, Apurba,Bandichhor, Rakeshwar

scheme or table, p. 6968 - 6970 (2012/02/13)

A novel approach to the synthesis of Boc-core, a key starting material for ritonavir and lopinavir involving an unprecedented diastereoselective nitroaldol reaction on β-amino aldehyde is disclosed.

HIV protease inhibiting compounds

-

Page/Page column 156, (2010/02/12)

A compound of the formula is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.

RETROVIRAL PROTEASE INHIBITING COMPOUNDS

-

, (2008/06/13)

A compound of the formula: STR1 is disclosed as an HIV protease inhibitor. Methods and compositions for inhibiting an HIV infection are also disclosed.

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