151294-93-8 Usage
Description
TERT-BUTYL 2-(TERT-BUTOXYCARBONYLAMINO)HEX-5-ENOATE is a versatile chemical compound derived from tert-butyl carbamate and hex-5-enoic acid. It is widely used in organic synthesis and pharmaceutical research, particularly as a protecting group for amino acids in peptide synthesis. Known for its role as an intermediate in the production of pharmaceuticals and agrochemicals, this compound requires careful handling due to its potential harmful effects if ingested or in direct contact with the skin.
Uses
Used in Organic Synthesis:
TERT-BUTYL 2-(TERT-BUTOXYCARBONYLAMINO)HEX-5-ENOATE is used as a protecting group for amino acids in peptide synthesis, facilitating the formation of complex peptide structures and enhancing the efficiency of the synthesis process.
Used in Pharmaceutical Research:
In the pharmaceutical industry, TERT-BUTYL 2-(TERT-BUTOXYCARBONYLAMINO)HEX-5-ENOATE serves as an intermediate in the development of various pharmaceuticals. Its unique chemical properties allow for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Production:
TERT-BUTYL 2-(TERT-BUTOXYCARBONYLAMINO)HEX-5-ENOATE is also utilized in the production of agrochemicals, contributing to the development of new pesticides, herbicides, and other agricultural chemicals that can improve crop yields and protect against pests.
Safety Precautions:
Due to its potential harmful effects, it is crucial to handle TERT-BUTYL 2-(TERT-BUTOXYCARBONYLAMINO)HEX-5-ENOATE with care, ensuring that it does not come into contact with the skin or is ingested. Proper safety measures, such as wearing protective gear and following established protocols, should be strictly adhered to when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 151294-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,9 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 151294-93:
(8*1)+(7*5)+(6*1)+(5*2)+(4*9)+(3*4)+(2*9)+(1*3)=128
128 % 10 = 8
So 151294-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H27NO4/c1-8-9-10-11(12(17)19-14(2,3)4)16-13(18)20-15(5,6)7/h8,11H,1,9-10H2,2-7H3,(H,16,18)
151294-93-8Relevant articles and documents
HEPATITIS C VIRUS INHIBITORS
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Page/Page column 97, (2012/03/08)
The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit RNA-containing virus, particularly the hepatitis C virus (HCV). Consequently, the compounds of the present invention
Beta-amino acid derivatives useful for the treatment of bacterial infections
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, (2008/06/13)
The invention provides compounds that are useful for the treatment of bacterial infections in mammals. More specifically, it is directed to beta-amino acid derivatives or pharmaceutically acceptable salts, prodrugs, or isomers of those compounds that are
Cross-metathesis of unsaturated α-amino acid derivatives
Biagini, Stefano C. G.,Gibson, Susan E.,Keen, Stephen P.
, p. 2485 - 2499 (2007/10/03)
Cross-metathesis of homoallylglycine derivatives with aryl- and alkyl-substituted alkenes using the ruthenium catalyst (Cy3P)2Cl2Ru=CHPh 1 has been achieved in 43-55 and 55-66% yield respectively. Allylglycine, vinylglycine and dehydroalanine derivatives have also been examined. Whilst cross-metathesis of allylglycine derivatives with alkyl-substituted alkenes using catalyst 1 may be regarded as a synthetically useful procedure, cross-metathesis reactions of vinylglycine and dehydroalanine derivatives using catalyst 1 are non-viable. Attachment of FmocHagOH 13 to a capped Wang resin, cross-metathesis with dodec-1-ene, and product removal from the resin gives the cross-metathesis product in 74% yield based on FmocHagOH.
