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Details

Stereochemistry ACHIRAL
Molecular Formula C5H11Br
Molecular Weight 151.045
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TERT-AMYL BROMIDE

SMILES

CCC(C)(C)Br

InChI

InChIKey=JOUWCKCVTDSMHF-UHFFFAOYSA-N
InChI=1S/C5H11Br/c1-4-5(2,3)6/h4H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C5H11Br
Molecular Weight 151.045
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Isomerization of neopentyl chloride and neopentyl bromide by a 1,2-interchange of a halogen atom and a methyl group.
2010-09-30
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:21:53 GMT 2025
Edited
by admin
on Mon Mar 31 21:21:53 GMT 2025
Record UNII
3NV4Z4Y7YV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-7897
Preferred Name English
TERT-AMYL BROMIDE
MI  
Systematic Name English
1,1-DIMETHYLPROPYL BROMIDE
Systematic Name English
2-METHYL-2-BROMOBUTANE
Systematic Name English
TERT-AMYL BROMIDE [MI]
Common Name English
TERT-PENTYL BROMIDE
Systematic Name English
2-BROMOISOPENTANE
Common Name English
2-BROMO-2-METHYLBUTANE
Systematic Name English
Code System Code Type Description
FDA UNII
3NV4Z4Y7YV
Created by admin on Mon Mar 31 21:21:53 GMT 2025 , Edited by admin on Mon Mar 31 21:21:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID5060146
Created by admin on Mon Mar 31 21:21:53 GMT 2025 , Edited by admin on Mon Mar 31 21:21:53 GMT 2025
PRIMARY
PUBCHEM
68180
Created by admin on Mon Mar 31 21:21:53 GMT 2025 , Edited by admin on Mon Mar 31 21:21:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-071-1
Created by admin on Mon Mar 31 21:21:53 GMT 2025 , Edited by admin on Mon Mar 31 21:21:53 GMT 2025
PRIMARY
MERCK INDEX
m1867
Created by admin on Mon Mar 31 21:21:53 GMT 2025 , Edited by admin on Mon Mar 31 21:21:53 GMT 2025
PRIMARY Merck Index
NSC
7897
Created by admin on Mon Mar 31 21:21:53 GMT 2025 , Edited by admin on Mon Mar 31 21:21:53 GMT 2025
PRIMARY
CAS
507-36-8
Created by admin on Mon Mar 31 21:21:53 GMT 2025 , Edited by admin on Mon Mar 31 21:21:53 GMT 2025
PRIMARY