Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H10N2 |
Molecular Weight | 122.1677 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(N)C=CC=C1N
InChI
InChIKey=RLYCRLGLCUXUPO-UHFFFAOYSA-N
InChI=1S/C7H10N2/c1-5-6(8)3-2-4-7(5)9/h2-4H,8-9H2,1H3
Molecular Formula | C7H10N2 |
Molecular Weight | 122.1677 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Biological monitoring of aromatic diisocyanates in workers exposed to thermal degradation products of polyurethanes. | 2002 Oct |
|
Development, validation and characterization of an analytical method for the quantification of hydrolysable urinary metabolites and plasma protein adducts of 2,4- and 2,6-toluene diisocyanate, 1,5-naphthalene diisocyanate and 4,4'-methylenediphenyl diisocyanate. | 2003 May-Aug |
|
Biological monitoring of exposure to toluene diisocyanate. | 2004 Oct |
|
Collaborative study on fifteen compounds in the rat-liver Comet assay integrated into 2- and 4-week repeat-dose studies. | 2010 Sep 30 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:47:27 GMT 2023
by
admin
on
Fri Dec 15 19:47:27 GMT 2023
|
Record UNII |
H838Q10551
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
H838Q10551
Created by
admin on Fri Dec 15 19:47:27 GMT 2023 , Edited by admin on Fri Dec 15 19:47:27 GMT 2023
|
PRIMARY | |||
|
76288
Created by
admin on Fri Dec 15 19:47:27 GMT 2023 , Edited by admin on Fri Dec 15 19:47:27 GMT 2023
|
PRIMARY | |||
|
13205
Created by
admin on Fri Dec 15 19:47:27 GMT 2023 , Edited by admin on Fri Dec 15 19:47:27 GMT 2023
|
PRIMARY | |||
|
212-513-9
Created by
admin on Fri Dec 15 19:47:27 GMT 2023 , Edited by admin on Fri Dec 15 19:47:27 GMT 2023
|
PRIMARY | |||
|
823-40-5
Created by
admin on Fri Dec 15 19:47:27 GMT 2023 , Edited by admin on Fri Dec 15 19:47:27 GMT 2023
|
PRIMARY | |||
|
147490
Created by
admin on Fri Dec 15 19:47:27 GMT 2023 , Edited by admin on Fri Dec 15 19:47:27 GMT 2023
|
PRIMARY | |||
|
4131
Created by
admin on Fri Dec 15 19:47:27 GMT 2023 , Edited by admin on Fri Dec 15 19:47:27 GMT 2023
|
PRIMARY | |||
|
DTXSID4027319
Created by
admin on Fri Dec 15 19:47:27 GMT 2023 , Edited by admin on Fri Dec 15 19:47:27 GMT 2023
|
PRIMARY | |||
|
C025235
Created by
admin on Fri Dec 15 19:47:27 GMT 2023 , Edited by admin on Fri Dec 15 19:47:27 GMT 2023
|
PRIMARY |