161402-83-1

• 

• Basic information

  1. Product Name: Ethanone, 1-(2,3-dihydroimidazo[2,1-b]thiazol-6-yl)- (9CI)
  2. Synonyms: Ethanone, 1-(2,3-dihydroimidazo[2,1-b]thiazol-6-yl)- (9CI)
  3. CAS NO:161402-83-1
  4. Molecular Formula: C7H8N2OS
  5. Molecular Weight: 168.21622
  6. EINECS: N/A
  7. Product Categories: ACETYLGROUP
  8. Mol File: 161402-83-1.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: Ethanone, 1-(2,3-dihydroimidazo[2,1-b]thiazol-6-yl)- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Ethanone, 1-(2,3-dihydroimidazo[2,1-b]thiazol-6-yl)- (9CI)(161402-83-1)
  11. EPA Substance Registry System: Ethanone, 1-(2,3-dihydroimidazo[2,1-b]thiazol-6-yl)- (9CI)(161402-83-1)

• 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: 161402-83-1(Hazardous Substances Data)

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161402-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161402-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,4,0 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 161402-83:
(8*1)+(7*6)+(6*1)+(5*4)+(4*0)+(3*2)+(2*8)+(1*3)=101
101 % 10 = 1
So 161402-83-1 is a valid CAS Registry Number.

161402-83-1Upstream product

• 1779-81-3 4,5-Dihydro-thiazol-2-ylamin 
• 61203-01-8 3-bromobut-3-en-2-one 

161402-83-1Downstream Products

161402-83-1Relevant articles and documents

SYNTHESIS OF 2,3,5,6-TETRAHYDROIMIDAZOTHIAZOLES

Kaugars, Girts,Martin, Scott E.,Nelson, Stephen J.,Watt, William

, p. 2593 - 2604 (1994)

The reactions of 2-amino-2-thiazoline with alkylating and acylating agents give initial reaction on the endocyclic nitrogen.Acyl groups, however, readily rearrange to the exocyclic nitrogen to give the products usually observed in these reactions.These observations clear up a considerable amount of confusion in the literature and lead to the efficient synthesis of 2,3,5,6-tetrahydroimidazothiazoles.

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