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[ CAS No. 107-41-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 107-41-5
Chemical Structure| 107-41-5
Structure of 107-41-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 107-41-5 ]

CAS No. :107-41-5 MDL No. :MFCD00004547
Formula : C6H14O2 Boiling Point : -
Linear Structure Formula :CH3CH(OH)CH2C(CH3)2OH InChI Key :SVTBMSDMJJWYQN-UHFFFAOYSA-N
M.W : 118.17 Pubchem ID :7870
Synonyms :
2-Methyl-2,4-pentanediol;MPD
Chemical Name :2-Methylpentane-2,4-diol

Safety of [ 107-41-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330 UN#:N/A
Hazard Statements:H302-H315-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 107-41-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 107-41-5 ]

[ 107-41-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 107-41-5 ]
  • [ 230299-21-5 ]
YieldReaction ConditionsOperation in experiment
98.6% With tetrakis(dimethylamido)diborane; In toluene; at 20 - 100℃; for 1.25h; HEXYLENEGLYCOL (2-methyl-2,4-pentanediol) (FW: 118. 18. 12.0 g, 101. 6 mmol) in toluene (40 mL) was treated with tetrakis (dimethylamino) diboron (FW: 197.926 ; 9.9 g, 50 mmol) at room temperature and the reaction mixture stirred. The temperature was raised to 100 C within 10 minutes while the release of dimethylamine started to occur after about 5 minutes. The temperature was maintained at 100 C. for 60 minutes at which time for 30 minutes the evolution of dimethylamine occurred. Toluene was removed to give a solid (99.6percent pure by GC). The solid was recrystallised from toluene: petroleum (80 C-100 C) (1: 9) to give a colourless solid of bis (hexylene glycolato) diboron (MF: C12H24B204 ; FW : 253.94) : 8. 83 g, second crop: 3.69 g, combined yield 12.52 g, 98. 6percent; 99.6percent pure by GC. mp 99-101. 6 C. 8 (CDC13, 200 MHz) 1.21 (d, J= 7Hz, 6H); 1.28 (s, 12H); 1.47 (dd, J=12,14 Hz, 2H); 1.70 (dd, J=14,3 Hz; 2H) 4.14 (dm, 2H) ppm. 13C 8 (CDCL3, 50 MHz) 23.1 ; 28.3 ; 31.2 ; 46. 2 ; 64.1 ; 70.3 ppm.
  • 2
  • [ 107-41-5 ]
  • diboronic ester [ No CAS ]
  • [ 230299-21-5 ]
YieldReaction ConditionsOperation in experiment
71% Example 16 4,4,4',4',6,6'-Hexamethyl-2,2'-bi-1,3,2-dioxaborinane This diboronic ester is prepared following general procedure A using 2-methyl-2,4-pentanediol. Yield, 71percent. 1H-nmr (CDCl3, 200 MHz): delta 1.18-1.32 (multiplet, 18H; 6*CH3), 1.44-1.56 (multiplet, 2H; 2*HCHC), 1.69-1.78 (multiplet, 2H; 2*HCHC) and 4.07-4.22 (multiplet, 2H; 2*OCH). F.W.: calc. for C12H24B2O4=253.94, found m/z 255 (M+1).
  • 3
  • [ 107-41-5 ]
  • [ 1630-79-1 ]
  • [ 230299-21-5 ]
  • 4
  • [ 107-41-5 ]
  • [ 952514-79-3 ]
  • 2-(4-(1-phenyl-1H-benzimidazol-2-yl)phenyl)-4,4,6-trimethyl-1,3,2-dioxaborinane [ No CAS ]
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