177963-76-7

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• Basic information

  1. Product Name: 3-Oxazolidinecarboxaldehyde, 2-(1-methylethyl)-5-oxo- (9CI)
  2. Synonyms: 3-Oxazolidinecarboxaldehyde, 2-(1-methylethyl)-5-oxo- (9CI)
  3. CAS NO:177963-76-7
  4. Molecular Formula: C7H11NO3
  5. Molecular Weight: 157.16714
  6. EINECS: N/A
  7. Product Categories: ALDEHYDE;ISOPROPYL
  8. Mol File: 177963-76-7.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: 3-Oxazolidinecarboxaldehyde, 2-(1-methylethyl)-5-oxo- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 3-Oxazolidinecarboxaldehyde, 2-(1-methylethyl)-5-oxo- (9CI)(177963-76-7)
  11. EPA Substance Registry System: 3-Oxazolidinecarboxaldehyde, 2-(1-methylethyl)-5-oxo- (9CI)(177963-76-7)

• 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: 177963-76-7(Hazardous Substances Data)

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• 3-Oxazolidinecarboxaldehyde, 2-(1-methylethyl)-5-oxo- (9CI)

  Cas No: 177963-76-7

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177963-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177963-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,9,6 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 177963-76:
(8*1)+(7*7)+(6*7)+(5*9)+(4*6)+(3*3)+(2*7)+(1*6)=197
197 % 10 = 7
So 177963-76-7 is a valid CAS Registry Number.

177963-76-7Upstream product

177963-76-7Downstream Products

177963-76-7Relevant articles and documents

Synthesis of 1-acylamino-1-(trimethylsiloxy)alkanes by trimethylsilyl trifluoromethanesulfonate-catalysed addition of bis(trimethylsilyl)amides to aldehydes

Johnson, A. Peter,Luke, Richard W. A.,Steele, Robert W.,Boa, Andrew N.

, p. 883 - 893 (2007/10/03)

Bis(trimethylsilyl)formamide reacts with aldehydes in refluxing chloroform, or at room temperature with catalysis by trimethylsilyl trifluoromethanesulfonate, to give 1-acylamino-1-(trimethylsiloxy)alkanes; similar results are obtained with other bis(trimethylsilyl)amides, but surprisingly not with bis(trimethylsilyl)acetamide, and addition of bis(trimethylsilyl)formamide to ketones and acetals can also be accomplished using TMS triflate as catalyst.

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