16573-72-1

• 

• Basic information

  1. Product Name: 4a,8a-Epoxynaphthalene,1,4,5,8-tetrahydro-(9CI)
  2. Synonyms: 4a,8a-Epoxynaphthalene,1,4,5,8-tetrahydro-(9CI)
  3. CAS NO:16573-72-1
  4. Molecular Formula: C₁₀H₁₂O
  5. Molecular Weight: 148.204
  6. EINECS: N/A
  7. Product Categories: EPOXYDE
  8. Mol File: 16573-72-1.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: 64 °C
  2. Boiling Point: 238.1±40.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.12±0.1 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 4a,8a-Epoxynaphthalene,1,4,5,8-tetrahydro-(9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 4a,8a-Epoxynaphthalene,1,4,5,8-tetrahydro-(9CI)(16573-72-1)
  11. EPA Substance Registry System: 4a,8a-Epoxynaphthalene,1,4,5,8-tetrahydro-(9CI)(16573-72-1)

• 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: 16573-72-1(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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16573-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16573-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,7 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16573-72:
(7*1)+(6*6)+(5*5)+(4*7)+(3*3)+(2*7)+(1*2)=121
121 % 10 = 1
So 16573-72-1 is a valid CAS Registry Number.

16573-72-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	4a,8a-Epoxynaphthalene,1,4,5,8-tetrahydro-(9CI)

1.2 Other means of identification

Product number	-
Other names	4A,8a-epoxy-1,4,4a,5,8,8a-hexahydro-naphthalene

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16573-72-1 SDS

16573-72-1Upstream product

• 493-04-9 isotetraline 
• 93-59-4 Perbenzoic acid 

16573-72-1Downstream Products

• 857051-86-6 9β-benzylthio-10α-hydroxy-1,4,5,8,9,10-hexahydronaphthalene 
• 857052-09-6 [2-(9β-benzylthio-1,2,3,4,5,6,7,8,9,10-decahydronaphthalen-10α-yloxy)-1-tert-butoxycarbonylmethoxymethylethoxy]-acetic acid tert-butyl ester 
• 857052-10-9 [2-(9β-benzylthio-1,2,3,4,5,6,7,8,9,10-decahydronaphthalen-10α-yloxy)-1-carboxymethoxymethylethoxy]-acetic acid 
• 857052-12-1 [2-(9β-benzylthio-1,2,3,4,5,6,7,8,9,10-decahydronaphthalen-10α-yloxy)-1-methoxymethylethoxy]-acetic acid tert-butyl ester 
• 857052-13-2 [2-(9β-benzylthio-1,2,3,4,5,6,7,8,9,10-decahydronaphthalen-10α-yloxy)-1-methoxymethylethoxy]-acetic acid 
• 857052-08-5 3-(9β-benzylthio-1,2,3,4,5,6,7,8,9,10-decahydronaphthalen-10α-yloxy)-1-O-methyl-propane-1,2-diol 
• 857052-07-4 3-(9β-benzylthio-1,2,3,4,5,6,7,8,9,10-decahydronaphthalen-10α-yloxy)-propane-1,2-diol 
• 857052-01-8 (9β-benzylthio-1,2,3,4,5,6,7,8,9,10-decahydronaphthalen-10α-yloxy)-acetic acid 
• 857052-06-3 2-(9β-benzylthio-1,2,3,4,5,6,7,8,9,10-decahydronaphthalen-10α-yloxy)-oxirane 
• 857052-05-2 9β-benzylthio-10α-allyloxy-1,2,3,4,5,6,7,8,9,10-decahydronaphthalene 
• 857051-99-1 9β-benzylthio-10α-hydroxy-1,2,3,4,5,6,7,8,9,10-decahydronaphthalene 
• 857051-84-4 9β-benzylsulfonyl-10α-hydroxy-1,4,5,8,9,10-hexahydronaphthalene 

16573-72-1Relevant articles and documents

Synthesis of anti-anti (anti-syn)-3,4:8,9-tetraacetoxy-11-oxa-tricyclo [4.4.1.01,6]undecanes

Kelebekli, Latif

, p. 94 - 97 (2011)

Synthesis of anti-anti-and anti-syn-3,4:8,9-tetraacetoxy-11-oxa-tricyclo[4. 4.1.01,6] undecanes have been achieved starting from naphthalene. The Birch reduction of naphthalene gave 1,4,5,8-tetrahydro-naphthalene in high yield. 1,4,5,8-Tetrahydro-naphthalene was selectively oxidised with mCPBA to give 11-oxa-tricyclo[4.4.1.01,6]undeca-3,8-diene. OsO4 oxidation followed by acetylation furnished the corresponding tetraacetates.

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