Home Cart Sign in  
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 135773-25-0 Chemical Structure| 135773-25-0

Structure of 135773-25-0

Chemical Structure| 135773-25-0

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 135773-25-0 ]

CAS No. :135773-25-0
Formula : C5H8IN3O2S
M.W : 301.11
SMILES Code : CN(C)S(=O)(=O)N1C=NC(I)=C1
MDL No. :MFCD02179543
InChI Key :HSJHNZMKMJPPGU-UHFFFAOYSA-N
Pubchem ID :2773390

Safety of [ 135773-25-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H331
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 135773-25-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 135773-25-0 ]

[ 135773-25-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 925-90-6 ]
  • [ 135773-25-0 ]
  • [ 31680-08-7 ]
  • [ 258527-71-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In diethyl ether; ethanol; dichloromethane; Example 11A 1H-imidazol-4-yl(4-methoxy-3-nitrophenyl)methanol A solution of 4-iodo-N,N-dimethyl-1H-imidazole-1-sulfonamide (3.0 g, 10 mmol) in dichloromethane (40 mL) under nitrogen was treated with ethylmagnesium bromide (3.0M in diethyl ether, 3.3 mL) over 2 minutes, stirred for 30 minutes, treated with 4-methoxy-5-nitrobenzaldehyde (2.0 g, 11 mmol), stirred for 1 hour, stored at 0 C. for 16 hours, concentrated to dryness, treated with 1 M HCl(100 mL), heated to 100 C. for 16 hours, cooled to ambient temperature, neutralized with NaHCO3 and extracted with 3:1 dichloromethane:ethanol (5*). The combined extractions were dried (MgSO4), filtered and concentrated. Purification on silica gel with 10% and then 20% ethanol/ammonia-saturated dichloromethane provided the desired compound. MS (DCI/NH3) m/z 250 (M+H)+.
With hydrogenchloride; In diethyl ether; ethanol; dichloromethane; EXAMPLE 11A 1H-imidazol-4-yl(4-methoxy-3-nitrophenyl)methanol A solution of 4-iodo-N,N-dimethyl-1H-imidazole-1-sulfonamide (3.0 g, 10 mmol) in dichloromethane (40 mL) under nitrogen was treated with ethylmagnesium bromide (3.0 M in diethyl ether, 3.3 mL) over 2 minutes, stirred for 30 minutes, treated with 4-methoxy-5-nitrobenzaldehyde (2.0 g, 11 mmol), stirred for 1 hour, stored at 0 C. for 16 hours, concentrated to dryness, treated with 1M HCl(100 mL), heated to 100 C. for 16 hours, cooled to ambient temperature, neutralized with NaHCO3 and extracted with 3:1 dichloromethane:ethanol (5*). The combined extractions were dried (MgSO4), filtered and concentrated. Purification on silica gel with 10% and then 20% ethanol/ammonia-saturated dichloromethane provided the desired compound. MS (DCI/NH3) m/z 250 (M+H)+.
 

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 135773-25-0 ]

Amines

Chemical Structure| 198127-92-3

A577378 [198127-92-3]

4,5-Diiodo-N,N-dimethyl-1H-imidazole-1-sulfonamide

Similarity: 0.91

Chemical Structure| 78162-58-0

A300878 [78162-58-0]

N,N-Dimethyl-1H-imidazole-1-sulfonamide

Similarity: 0.84

Sulfamides

Chemical Structure| 198127-92-3

A577378 [198127-92-3]

4,5-Diiodo-N,N-dimethyl-1H-imidazole-1-sulfonamide

Similarity: 0.91

Chemical Structure| 78162-58-0

A300878 [78162-58-0]

N,N-Dimethyl-1H-imidazole-1-sulfonamide

Similarity: 0.84

Iodides

Chemical Structure| 198127-92-3

A577378 [198127-92-3]

4,5-Diiodo-N,N-dimethyl-1H-imidazole-1-sulfonamide

Similarity: 0.91