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Details

Stereochemistry ACHIRAL
Molecular Formula C4H6O
Molecular Weight 70.0898
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-BUTYNOL

SMILES

CC#CCO

InChI

InChIKey=NEEDEQSZOUAJMU-UHFFFAOYSA-N
InChI=1S/C4H6O/c1-2-3-4-5/h5H,4H2,1H3

HIDE SMILES / InChI

Molecular Formula C4H6O
Molecular Weight 70.0898
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Acyclic nucleoside analogues as novel inhibitors of human mitochondrial thymidine kinase.
2002 Sep 12
Acetylenic TACE inhibitors. Part 2: SAR of six-membered cyclic sulfonamide hydroxamates.
2005 Oct 1
Synthesis and activity of quinolinylmethyl P1' alpha-sulfone piperidine hydroxamate inhibitors of TACE.
2009 Jul 1
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 07:55:44 GMT 2023
Edited
by admin
on Sat Dec 16 07:55:44 GMT 2023
Record UNII
US5293942K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-BUTYNOL
Systematic Name English
2-BUTYN-1-OL
Systematic Name English
2-BUTYNYL ALCOHOL
Systematic Name English
NSC-222371
Code English
1-HYDROXYBUT-2-YNE
Systematic Name English
Code System Code Type Description
PUBCHEM
12991
Created by admin on Sat Dec 16 07:55:44 GMT 2023 , Edited by admin on Sat Dec 16 07:55:44 GMT 2023
PRIMARY
ECHA (EC/EINECS)
212-113-4
Created by admin on Sat Dec 16 07:55:44 GMT 2023 , Edited by admin on Sat Dec 16 07:55:44 GMT 2023
PRIMARY
FDA UNII
US5293942K
Created by admin on Sat Dec 16 07:55:44 GMT 2023 , Edited by admin on Sat Dec 16 07:55:44 GMT 2023
PRIMARY
CAS
764-01-2
Created by admin on Sat Dec 16 07:55:44 GMT 2023 , Edited by admin on Sat Dec 16 07:55:44 GMT 2023
PRIMARY
EPA CompTox
DTXSID8022115
Created by admin on Sat Dec 16 07:55:44 GMT 2023 , Edited by admin on Sat Dec 16 07:55:44 GMT 2023
PRIMARY
NSC
222371
Created by admin on Sat Dec 16 07:55:44 GMT 2023 , Edited by admin on Sat Dec 16 07:55:44 GMT 2023
PRIMARY