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Detail of "115-76-4"

  • CAS Number:
  • 115-76-4
  • Name:
  • 1,3-Propanediol,2,2-diethyl-

  • Superlist Name:
  • 2,2-Diethylpropanediol
  • Molecular Structure:
  • Formula:
  • C7H16O2
  • Molecular Weight:
  • 132.23
  • Synonyms:
  • 2,2-Diethyl-1,3-propanediol;DMP;NSC 12211;NSC 169507;Prenderol;2,2-Diethylpropane-1,3-diol;Di-aethyl-propanediol;3,3-Bis(hydroxymethyl)pentane;
  • EINECS:
  • 204-103-3
  • Density:
  • 0.95 g/cm3
  • Melting Point:
  • 59-61 °C(lit.)
  • Boiling Point:
  • 240.499 °C at 760 mmHg
  • Flash Point:
  • 101.139 °C
  • Appearance:
  • white to slightly yellow crystalline powder
  • Hazard Symbols:
  • HarmfulXn
  • Risk Codes:
  • 22-36
  • Safety:
  • 26 Details

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CAS No.115-76-4 2,2-Diethylpropanediol

Supplier:Sarchem Laboratories, Inc. [ United States]

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CAS No.115-76-4 2,2-Diethylpropanediol

2,2-DIETHYL-1,3-PROPANEDIOL

Supplier:ChemService Inc. [ United States]

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Address:PO Box 599 West Chester, PA 19381-0599 USA

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CAS No.115-76-4 2,2-Diethylpropanediol

2,2-DIETHYL-1,3-PROPANEDIOL

Supplier:Narchem Corporation [ United States]

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Address:3800 West 38th Street Chicago, IL 60632-3311

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CAS No.115-76-4 2,2-Diethylpropanediol

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Supplier:Tianjin Guangfu Fine Chemical Research Institute [ China (Mainland)]

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Tel:022-27918488

Address:Tianjing

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CAS No.115-76-4 2,2-Diethylpropanediol

Supplier:CHEMSWORTH [ India]

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Tel:+91-261-2397244

Address:Unit.133 & 134, Plot 256, Surat Special Economic Zone,Sachin- 394 230

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Reference

Decomposition of carbonate esters of 1,3-diols
Decomposition of carbonate esters of 1,3-diols. The chemistry of 1,3-bifunctional systems. XXVI. Bartok, M.; Molnar, A.; Bartok-Bozoki, G. (Dep. 17361-58-9 and 115-76-4 are cas registry numbers. These chemicals are also mentioned in this article. Org. Chem., Jozsef Attila Univ., Szeged H-6720, Hung.). Acta Chim. Hung., 114(3-4), 375-9 (English) 1983. CODEN: ACHUDC. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) The decompn. of cyclic carbonates I (n = 0, 1) and II, as well as MeCH(OH)(CH2)nOH (n = 1, 2) and Et2C(CH2OH)2, was examd. in the presence of KOH, KCN, and LiCl. With a large excess of KOH, I and II are transformed into alcs. contg. one C less than their corresponding diols. Other reactions, which are known, include fragmentation to oxo compds., CO2 elimination to give oxetanes, and fragmentation to olefins. .
Preparation of cyclic carbonates and 2-oxazolidones using di-2-pyridyl carbonate
Preparation of cyclic carbonates and 2-oxazolidones using di-2-pyridyl carbonate. Kim, Sunggak; Ko, Young Kwan (Dep. Chem., Korea Adv. Inst. Sci. Technol., Seoul 131, S. Korea). Heterocycles, 24(6), 1625-30 (English) 1986. CODEN: HTCYAM. ISSN: 0385-5414. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Cyclic carbonates, e.g., I (n = 1,2) and oxazolidinones, e.g., II (R = Me, Ph, R1 = H; R = H, R1 = Et) were conveniently prepd. in 80-96% yields by the reaction of diols and b-amino alcs.In this experiment, several chemicals are used like 115-76-4 resp. with di-2-pyridyl carbonate. .
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