19981-17-0

Basic information

• Product Name: cyanamide, sodium salt
• Synonyms: cyanamide, sodium salt;Cyanamide/sodium,(1:x) salt
• CAS NO: 19981-17-0
• Molecular Formula: CHN₂*Na
• Molecular Weight: 64.02181
• EINECS: 243-451-0
• Mol File: 19981-17-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: cyanamide, sodium salt(CAS DataBase Reference)
• NIST Chemistry Reference: cyanamide, sodium salt(19981-17-0)
• EPA Substance Registry System: cyanamide, sodium salt(19981-17-0)

Safety Data

• Hazardous Substances Data: 19981-17-0(Hazardous Substances Data)

Usage

InChI:InChI=1/CH2N2.Na/c2-1-3;/h2H2;/q;+1

Upstream product

• 57-13-6 urea 
• 100-47-0 benzonitrile 
• 65-85-0 benzoic acid 
• 815-24-7 Di-t-butyl ketone 
• 56-23-5 tetrachloromethane 
• 74-90-8 hydrogen cyanide 
• 460-19-5 ethanedinitrile 
• 137-40-6 sodium proprionate 
• 2922-54-5 sodium hydrogen succinate 
• 62-76-0 sodium oxalate 
• 102-07-8 bis(diphenyl)urea 
• 7681-38-1 sodium hydrogen sulfate 
• 156-62-7 calcium hydrogencyanamide 
• 590-29-4 potassium formate 

Downstream Products

• 24665-93-8 4,5-dihydro-oxazol-2-ylamine 
• 1934-75-4 sodium dicyanamide 
• 766-94-9 vinyl phenyl ether 
• 5863-82-1 1-ethyl 2,4-dithiobiuret 
• 5848-27-1 N-cyano-N'-isopropyl-S-methyl-isothiourea 
• 76989-89-4 sodium salt of 1-cyanourea 
• 15150-25-1 N-cyanobenzamide 
• 41834-91-7 3-phenyl-1-ureidonitrile 
• 41835-08-9 N-cyano-N'-phenylthiourea 
• 538-08-9 Diallylcyanamid 
• 5848-24-8 S-methyl-N-cyano-N'-methyl-carbamimidothioate 
• 16724-63-3 dihexadecylamine 
• 103818-49-1 N-carbobenzoxyglycylcyanamide 
• 114658-32-1 Z-L-leucylcyanamide 

Relevant articles and documents

Sulfoxide-to-sulfilimine conversions: Use of modified Burgess-type reagents

Sulfoxides can directly be converted into N-cyanosulfilimines using a new Burgess-type reagent. By applying this strategy with a related reagent variant, synthetically valuable NH-sulfoximines have been prepared from sulfoxides via N-protected sulfilimines. The practical three-step reaction sequence is generally high yielding and applicable to a wide range of substrates. The sulfoxide-to-sulfilimine conversion can also be performed under solvent-reduced conditions in a ball mill. Copyright

Compounds derived from an amine nucleus and pharmaceutical compositions comprising same

Compounds having the formula (I), are effective as inhibitors of IMPDH enzyme and/or serine protease Factor VIIa, wherein B is a monocyclic or bicyclic carbocyclic or heterocyclic ring, D is a monocyclic or bicyclic carbocyclic or heterocyclic ring except when A is a heterocyclic ring, then D is a heterocyclic ring system, R is hydrogen or C1-4alkyl, and A, R1, R2 and R4 are as defined in the specification.

Inhibitors of IMPDH enzyme

The present invention discloses the identification of the novel inhibitors of IMPDH (inosine-5′-monophosphate dehydrogenase). The compounds and pharmaceutical compositions disclosed herein are useful in treating or preventing IMPDH-associated disorders, such as transplant rejection and autoimmune diseases.