14683-75-1

• 

• Basic information

  1. Product Name: diethoxy-hexan-2-yloxy-sulfanylidene-phosphorane
  2. Synonyms: diethoxy-hexan-2-yloxy-sulfanylidene-phosphorane
  3. CAS NO:14683-75-1
  4. Molecular Formula: C10H23O3PS
  5. Molecular Weight: 254.326581
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 14683-75-1.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 273.7°Cat760mmHg
  3. Flash Point: 119.3°C
  4. Appearance: /
  5. Density: 1.037g/cm³
  6. Vapor Pressure: 0.00946mmHg at 25°C
  7. Refractive Index: 1.464
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: diethoxy-hexan-2-yloxy-sulfanylidene-phosphorane(CAS DataBase Reference)
  11. NIST Chemistry Reference: diethoxy-hexan-2-yloxy-sulfanylidene-phosphorane(14683-75-1)
  12. EPA Substance Registry System: diethoxy-hexan-2-yloxy-sulfanylidene-phosphorane(14683-75-1)

• 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: 14683-75-1(Hazardous Substances Data)

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14683-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14683-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,8 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14683-75:
(7*1)+(6*4)+(5*6)+(4*8)+(3*3)+(2*7)+(1*5)=121
121 % 10 = 1
So 14683-75-1 is a valid CAS Registry Number.

InChI:InChI=1/C10H23O3PS/c1-5-8-9-10(4)13-14(15,11-6-2)12-7-3/h10H,5-9H2,1-4H3

14683-75-1SDS

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	diethoxy-hexan-2-yloxy-sulfanylidene-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number	-
Other names	Thiophosphorsaeure-O,O'-diaethylester-S-hexylester

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:14683-75-1 SDS

14683-75-1Upstream product

• 5871-17-0 potassium O,O'-diethylthiophosphate 
• 111-25-1 1-bromo-hexane 
• 28519-32-6 4-Methylbenzolthiosulfonsaeure-S-hexylester 
• 122-52-1 triethyl phosphite 
• 111-31-9 Hexanethiol 
• 762-04-9 phosphonic acid diethyl ester 
• 6803-40-3 1-hexylthiocyanate 
• 2303-76-6 sodium diethyl phosphite 
• 638-45-9 1-Iodohexane 
• 544-10-5 1-Chlorohexane 

14683-75-1Downstream Products

14683-75-1Relevant articles and documents

SYNTHESIS AND ANTICHOLINE ESTERASE PROPERTIES OF S-ETYNYL ESTERS OF THIOPHOSPHORIC ACIDS

Godovikov, N. N.,Vikhreva, L. A.,Babasheva, K. K.,Sherstobitov, O. E.,Balashova, E. K.,et al.

, p. 1453 - 1455 (1983)

-

Base-controlled Fe(Pc)-catalyzed aerobic oxidation of thiols for the synthesis of S-S and S-P(O) bonds

Huang, Hai,Ash, Jeffrey,Kang, Jun Yong

, p. 4236 - 4242 (2018/06/21)

Fe(Pc)-Catalyzed aerobic oxidation of thiols for the synthesis of disulfides has been developed under mild reaction conditions. In addition, an aerobic oxidative cross-dehydrogenative coupling (CDC) reaction of thiols with P(O)-H compounds (H-phosphonates and H-phosphine oxide) for the formation of S-P(O) bonds has been demonstrated under the Fe(Pc) catalysis system with a base additive. Control experiments revealed that the use of a base (DIPA) in this system controls the synthetic pathways in which thiophosphates are formed.

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