299175-13-6

• 

• Basic information

  1. Product Name: Acetamide, N-[[[(dimethylamino)methylene]amino]thioxomethyl]-N-methyl-
  2. Synonyms: Acetamide, N-[[[(dimethylamino)methylene]amino]thioxomethyl]-N-methyl-
  3. CAS NO:299175-13-6
  4. Molecular Formula: C7H13N3OS
  5. Molecular Weight: 0
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 299175-13-6.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Acetamide, N-[[[(dimethylamino)methylene]amino]thioxomethyl]-N-methyl-(CAS DataBase Reference)
  10. NIST Chemistry Reference: Acetamide, N-[[[(dimethylamino)methylene]amino]thioxomethyl]-N-methyl-(299175-13-6)
  11. EPA Substance Registry System: Acetamide, N-[[[(dimethylamino)methylene]amino]thioxomethyl]-N-methyl-(299175-13-6)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 299175-13-6(Hazardous Substances Data)

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299175-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 299175-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,1,7 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 299175-13:
(8*2)+(7*9)+(6*9)+(5*1)+(4*7)+(3*5)+(2*1)+(1*3)=186
186 % 10 = 6
So 299175-13-6 is a valid CAS Registry Number.

299175-13-6Upstream product

• 75-36-5 acetyl chloride 

299175-13-6Downstream Products

299175-13-6Relevant articles and documents

2,4-Diamino-1-thia-3-azabutadienes, intermediates in heterocyclic synthesis

Friot,Reliquet,Reliquet,Meslin

, p. 135 - 149 (2007/10/03)

2,4-Diamino-1-thia-3-azabutadienes 1 were studied. Methylation occured at sulfur and acylation at nitrogen hound to the 2 position. Alkylation by α-bromoketones gave rise to 2-amino-5-acylthiazoles. Upon treatment with acrylic dienophiles compounds 1 reac

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