ChemicalBook > CAS DataBase List > N-Iodosuccinimide

N-Iodosuccinimide

Product Name
N-Iodosuccinimide
CAS No.
516-12-1
Chemical Name
N-Iodosuccinimide
Synonyms
NIS;1-iodopyrrolidine-2,5-dione;Iodosuccinimide;N-IodosucciniMide (NIS);1-IODO-2,5-PYRROLIDINEDIONE;N-iododiimide;succiniodimide;N-IODOSUCCINIMIDE;n-iodo-succinimid;N-lodosuccinimide
CBNumber
CB0342078
Molecular Formula
C4H4INO2
Formula Weight
224.98
MOL File
516-12-1.mol
More
Less

N-Iodosuccinimide Property

Melting point:
202-206 °C(lit.)
Boiling point:
249.6±23.0 °C(Predicted)
Density 
2,245 g/cm3
storage temp. 
2-8°C
solubility 
Soluble in dioxane, tetrahydrfuran and acetonitrile. Insoluble in ether and carbon tetrachloride.
pka
-2.57±0.20(Predicted)
form 
Crystalline Powder
color 
White-yellow to brown
Water Solubility 
decomposes
Sensitive 
Moisture Sensitive
Merck 
14,5045
BRN 
113917
Stability:
Moisture Sensitive
InChIKey
LQZMLBORDGWNPD-UHFFFAOYSA-N
CAS DataBase Reference
516-12-1(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
RTECS 
WN2817000
8-9
Hazard Note 
Harmful/Keep Cold/Moisture Sensitive
TSCA 
No
HazardClass 
IRRITANT
HS Code 
29251995
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H341Suspected of causing genetic defects

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P308+P313IF exposed or concerned: Get medical advice/attention.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
220051
Product name
N-Iodosuccinimide
Purity
95%
Packaging
5g
Price
$58.9
Updated
2024/03/01
Sigma-Aldrich
Product number
220051
Product name
N-Iodosuccinimide
Purity
95%
Packaging
25g
Price
$126
Updated
2024/03/01
TCI Chemical
Product number
I0074
Product name
N-Iodosuccinimide
Purity
>98.0%(T)
Packaging
5g
Price
$47
Updated
2024/03/01
TCI Chemical
Product number
I0074
Product name
N-Iodosuccinimide
Purity
>98.0%(T)
Packaging
25g
Price
$134
Updated
2024/03/01
Alfa Aesar
Product number
A14320
Product name
N-Iodosuccinimide, 97%
Packaging
5g
Price
$53.1
Updated
2024/03/01
More
Less

N-Iodosuccinimide Chemical Properties,Usage,Production

Chemical Properties

white-yellow to brown crystalline powder

Uses

Iodination of ketones and aldehydes.
Highly substituted iodobenzenes prepared via an efficient 2-step process from 1,6-diynes.
Used with TFA to chemoselectively hydrolyze thioglycosides to 1-hydroxyglycosides.
Synthesis of vinyl sulfones from olefins and benzenesulfinic acid.

Uses

N-Iodosuccinimide is used in the preparation of vinyl sulfones from olefins and benzenesulfinic acid. It acts as a source for I+ and involved in Hunsdiecker reactions for the conversion of cinnamic acids, and propiolic acids to the corresponding alfa-halostyrenes and 1-halo-1-alkynes respectively. It is also used to hydrolyze thioglycosides to 1-hydroxyglycosides with triluoroacetic acid. It is involved in the preparation of iodobenzene from 1,6-diynes. Further, it acts as an iodinating agent in chemical synthesis.

Uses

N-Iodosuccinimide is a iodo substituted succinimide that is used as an iodinating agent in chemical synthesis.

Preparation

To a solution of 39.2g of succinimide in 1200ml of boiling water was added 51.0g of freshly precipitated silver oxide, the mixture was filtered and the silver salt was allowed to crystallize. Filtration and washing with cold water furnished 45.0g of the silver salt of succinimide suitable for the iodination step.
The finely powdered salt (49.5g) was added in portions with stirring to a solution of 50.8g of iodine in 300ml of acetone, the temperature being maintained at 5-10°C. After decolorization (30 min.), the silver iodide was filtered, the solvent was removed under reduced pressure at room temperature and the residue was washed with ether, yielding 43g of N-iodosuccinimide with mp 189-191°C. An analytical sample (85% recovery) was obtained by dissolving in the minimum quantity of hot dioxane and precipitating with carbon tetrachloride; colorless needles, mp 200-201°C.
Ref: JACS 75, 3493 (1953)

Definition

ChEBI: N-iodosuccinimide is a five-membered cyclic dicarboximide compound having an iodo substituent on the nitrogen atom. It is a dicarboximide and a pyrrolidinone. It derives from a succinimide.

Reactions

N-Iodosuccinimide (NIS) is an iodinating agent that is used for various electrophilic iodinations and as source for iodine in radical reactions.
N-Iodosuccinimide is the least reactive of the N-haloamides in aromatic substitution. N-Iodosuccinimide does not act as an iodinating agent in pure dimethyl sulfoxide or N-ethylacetamide. On the other hand, butyl disulfide and a number of other sulfur-containing compounds are effective catalysts at low concentration for the iodination of guanosine derivatives using N-iodosuccinimide. This catalytic effect is observed when dimethyl sulfoxide is used as the solvent,but not when N-ethylacetamide is used.
https://www.organic-chemistry.org/chemicals/oxidations/n-iodosuccinimide-nis.shtm

Synthesis Reference(s)

Journal of the American Chemical Society, 75, p. 3493, 1953 DOI: 10.1021/ja01110a055
Organic Syntheses, Coll. Vol. 5, p. 663, 1973
Tetrahedron Letters, 25, p. 233, 1984 DOI: 10.1016/S0040-4039(00)99848-4

Purification Methods

Crystallise it from dioxane/CCl4. It iodinates arenes in triflic acid. [Olah et al J Org Chem 58 3194 1993, Beilstein 21/9 V 544.]

N-Iodosuccinimide Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

N-Iodosuccinimide Suppliers

Apollo Scientific Ltd.
Tel
--
Fax
--
Email
sales@apolloscientific.co.uk
Country
United Kingdom
ProdList
6084
Advantage
88
CMS Chemicals Limited
Tel
--
Fax
--
Email
cms.marketing@cms-chemicals.com
Country
United Kingdom
ProdList
3708
Advantage
60
Tokyo Chemical Industry UK Ltd.
Tel
--
Fax
--
Email
sales@tci-uk.co.uk
Country
United Kingdom
ProdList
1637
Advantage
50
Apin Chemicals Limited (UK)
Tel
--
Fax
--
Email
info@apinchemicals.com
Country
United Kingdom
ProdList
6184
Advantage
60
Carbosynth Limited
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6581
Advantage
61
Leancare Ltd.
Tel
--
Fax
--
Email
enquiry@leancare.co.uk
Country
United Kingdom
ProdList
6446
Advantage
42
Hawks Scientific Ltd
Tel
--
Fax
--
Email
pete@hawks-scientific.com
Country
United Kingdom
ProdList
2221
Advantage
43
CARBONE SCIENTIFIC CO.,LTD
Tel
--
Fax
--
Email
sales@carbonesci.com
Country
United Kingdom
ProdList
6666
Advantage
30
Eurolabs Limited
Tel
--
Fax
--
Country
United Kingdom
ProdList
6309
Advantage
46
MOLEKULA Ltd.
Tel
--
Fax
--
Email
kevinbanks@molekula.com
Country
United Kingdom
ProdList
6140
Advantage
66
UK GREEN SCIENTIFIC CO.,LIMITED
Tel
--
Fax
--
Email
sales@gs-chem.com
Country
United Kingdom
ProdList
6098
Advantage
47
Fluorochem Ltd
Tel
--
Fax
--
Email
vernam@fluorochem.co.uk
Country
United Kingdom
ProdList
6375
Advantage
65
ARIAC - Armenian Institute of Applied Chemistry
Tel
--
Fax
--
Email
ariac@web.am
Country
United Kingdom
ProdList
2466
Advantage
46
ProSynth Ltd
Tel
--
Fax
--
Country
United Kingdom
ProdList
1005
Advantage
51
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United Kingdom
ProdList
6401
Advantage
74
Apin Chemicals Ltd.
Tel
--
Fax
--
Email
info@apinchemicals.com
Country
United Kingdom
ProdList
6807
Advantage
42
VWR International
Tel
--
Fax
--
Email
solutions@vwr.com
Country
United Kingdom
ProdList
6548
Advantage
82
More
Less

View Lastest Price from N-Iodosuccinimide manufacturers

HebeiShuoshengImportandExportco.,Ltd
Product
N-Iodosuccinimide 516-12-1
Price
US $6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000KG/Month
Release date
2024-08-05
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
N-Iodosuccinimide 516-12-1
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-05-06
Hebei Longbang Technology Co., Ltd
Product
N-Iodosuccinimide 516-12-1
Price
US $6.00/kg
Min. Order
1kg
Purity
More than 99%
Supply Ability
2000KG/Month
Release date
2024-05-27

516-12-1, N-IodosuccinimideRelated Search:


  • 1-iodo-5-pyrrolidinedione
  • 1-IODO-2,5-PYRROLIDINEDIONE
  • NIS
  • N-IODOSUCCINIMIDE
  • N-Iodosuccinimide, 98+%
  • N-Iodosuccinimide ,99%
  • N-Iodosuccinimide , (1-Iodo-2,5-pyrrolidinedione)
  • 1-Iodopyrrolidine-2,5-dione, 2,5-Dioxo-1-iodopyrrolidine
  • N-IodosucciniMide (NIS)
  • N-IodosucciniMide, 98% 100GR
  • N-IodosucciniMide, 98% 10GR
  • N-iodobutanimide/NIS
  • N-IodosucciniMide / N-IodobutaniMide
  • N-iodoDing twoiMide
  • N - butyl diiMide iodine generation
  • <i>N</i>-Iodosuccinimide
  • 1-iodopyrrolidine-2,5-dione
  • Iodosuccinimide
  • 2,5-Pyrrolidinedione, 1-iodo-
  • N-Iodosuccinimide, 97+%
  • n-iodo-succinimid
  • Succinimide,N-iodo-
  • succiniodimide
  • N-Iodosuccinimide≥ 99.9% (Iodometry)
  • N-Iodosuccinimide, 97%, for synthesis
  • N-Iodosuccinimide&gt
  • N-IODOSUCCINIMIDE FOR SYNTHESIS
  • N-succinimide (NIS)
  • N-iododiimide
  • N-iodosuccinimideb
  • Big Discount Purity 99% N-Iodosuccinimide CAS 516-12-1 with Best Quality
  • Intermediate Material N-Iodosuccinimide (NIS) CAS?516-12-1
  • N-Iodosuccinimide 5GM
  • N-Iodosuccinimide extrapure, 99%
  • IODOSUCCINIMIDE For Synthesis
  • N-lodosuccinimide
  • Ripretinib Impurity 39
  • N-Iodosuccinimide (1-Iodopyrrolidine-2,5-Dione)
  • 516-12-1
  • 208-221-6
  • 512-12-1
  • C4H4INO2
  • C4H4O2NI
  • Reagents for Oligosaccharide Synthesis
  • Iodination
  • N-Substituted Succinimides
  • N-Substituted Maleimides, Succinimides & Phthalimides
  • Halogenation
  • C-X Bond Formation (Halogen)
  • Synthetic Reagents
  • C-X Bond Formation (Halogen)
  • Synthetic Reagents
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • API intermediates
  • Biochemistry
  • Halogenation
  • Iodination
  • N-Substituted Maleimides, Succinimides & Phthalimides