Iodoac­etamide CAS 144-48-9

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• Prop­er­ties
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Iden­ti­fi­ca­tion

CAS Number

144-48-9

Name

Iodoac­etamide

Syn­onyms

144-48-9 [RN]
205-630-1 [EINECS]
2-Iodac­e­tamid [Ger­man] [ACD/IUPAC Name]
2-Iodoac­e­tamide [ACD/IUPAC Name]
2-Iodoacé­­tamide [French] [ACD/IUPAC Name]
AC4200000
Acetamide, 2-iodo- [ACD/​Index Name]
Iodoac­etamide [Wiki]
ZRH8M27S79
[144-48-9]
205-630-1MFCD00008028
215-742-2 [EINECS]
24072-75-1 [RN]
2-iodanylethanamide
2-Iodo-acetamide
2-iodoac­e­tamide (ACD/​Name 4.0)
2-iodoac­e­tamide 99%
2-iodoac­e­tamide, crys­tal
2-iodoacetamide,98%
2-iodoethanamide
4-02-00-00536 (Beil­stein Hand­book Ref­er­ence) [Beil­stein]
Acetamide, 2-iodo- (8CI,9CI)
Acetamide, iodo- (6CI)
a-Iodoac­e­tamide
C2H4INO
D007460
EINECS 205-630-1
http:////www.amadischem.com/proen/486910/
IAM
iam,iodoacetamide
iodac­etamide
iodioac­etamide
-iodoac­etamide
iodoac­etamide 98%
iodoacetamide(rs20011038)
iodoac­etamide, 98%
IODOAC­E­TAMIDE-15N
Iodoace­toamide
iodoacetoamide|2-iodoacetamide|acetamide, 2-iodo-|monoiodoacetamide|surauto|N-(3-methoxy-4-butoxybenzyl)thiobarbituric acid
lodoac­etamide
Lopac0_​000570
Methyl α-D-glu­­co­­side [VAN]
MONOIODOAC­ETAMIDE
N-(3-Methoxy-4-butoxybenzyl)thiobarbituric acid
nchembio.146-comp6
PI-47045
Sjyhcaviktp@
ST-9100
Surauto
UNII :ZRH8M27S79
UNII-ZRH8M27S79
WLN : ZV1I
α-iodo acetamide
α-iodoac­e­tamide
α-Iodoac­e­tamide
α-Iodoac­e­tamide
α-Iodoac­e­tamide – CAS 144-48-9 – Cal­biochem
ヨードアセトアミド [Japan­ese]

SMILES

C(C(=N)O)I

Std­InChI

InChI=1S/C2H4INO/c3-1-2(4)5/h1H2,(H2,4,5)

Std­InChIKey

PGLTVOM­IX­­TU­U­RA-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C₂H₄INO 

Mol­e­c­u­lar Weight

184.96

EINECS

205-630-1

MDL Number

MFCD00008028

Prop­er­ties

Appear­ance

White Crys­talline

Melt­ing Point

92-95°C

Safe­ty Data

Sym­bol

GHS06

Sig­nal Word

Dan­ger

Haz­ard statements

Pre­cau­tion­ary Statements

WGK Germany

3

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our Iodoac­etamide CAS 144-48-9

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

Puri­ty

98% min

Shelf Life

2 years

Stor­age

Under room tem­per­a­ture away from light

Known Appli­ca­tion

In pro­teomics, his­ti­dine and cys­teine alky­la­tion reagents are used for pep­tide sequenc­ing and enzyme inhibitors ; it is also used for organ­ic synthesis.

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