Details
Stereochemistry | ACHIRAL |
Molecular Formula | CH2IO3S.Na |
Molecular Weight | 243.984 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[O-]S(=O)(=O)CI
InChI
InChIKey=COCJIVDXXCJXND-UHFFFAOYSA-M
InChI=1S/CH3IO3S.Na/c2-1-6(3,4)5;/h1H2,(H,3,4,5);/q;+1/p-1
Molecular Formula | Na |
Molecular Weight | 22.9898 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | CH2IO3S |
Molecular Weight | 220.994 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/4377903
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4377903
Methiodal is used in lumbar myelography as a contrast agent.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:04:19 GMT 2023
by
admin
on
Fri Dec 15 15:04:19 GMT 2023
|
Record UNII |
3880P18UBM
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C28500
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
126-31-8
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
204-782-6
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
23662381
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
C100285
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
DTXSID701035794
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
1881
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
100000081412
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
SUB08848MIG
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
510652
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
C83954
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
m7315
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | Merck Index | ||
|
3880P18UBM
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
4377
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY | |||
|
CHEMBL2110978
Created by
admin on Fri Dec 15 15:04:19 GMT 2023 , Edited by admin on Fri Dec 15 15:04:19 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |