Top quality factory supply 41051-72-3 2-METHYL-1,2-BUTANEDIOL at low price
- Molecular Formula:C5H12 O2
- Molecular Weight:104.149
- Vapor Pressure:0.237mmHg at 25°C
- Refractive Index:1.4480
- Boiling Point:182.3°Cat760mmHg
- PKA:14.56±0.29(Predicted)
- Flash Point:78.5°C
- PSA：40.46000
- Density:0.981g/cm3
- LogP:0.13970
2-METHYL-1,2-BUTANEDIOL(Cas 41051-72-3) Usage
|
Definition |
ChEBI: A glycol that is 1,2-butanediol carrying an additional methyl substituent at position 2. |
InChI:InChI=1/C5H12O2/c1-3-5(2,7)4-6/h6-7H,3-4H2,1-2H3
41051-72-3 Relevant articles
Biotransformation of [12C]- and [13C]-tert-amyl methyl ether and tert-amyl alcohol
Amberg, Alexander,Bernauer, Ulrike,Scheutzow, Dieter,Dekant, Wolfgang
, p. 958 - 964 (1999)
tert-Amyl methyl ether (TAME) is intende...
1. 2 - O-alcohol synthetic method of the compound (by machine translation)
-
Paragraph 0039; 0040, (2019/03/17)
The invention relates to a 1, 2 - O-alco...
Total synthesis and absolute configuration of avenolide, extracellular factor in Streptomyces avermitilis
Uchida, Miho,Takamatsu, Satoshi,Arima, Shiho,Miyamoto, Kiyoko T,Kitani, Shigeru,Nihira, Takuya,Ikeda, Haruo,Nagamitsu, Tohru
experimental part, p. 781 - 787 (2012/06/16)
The first total synthesis of extracellul...
2,3,5-TRISUBSTITUTED PYRIDINES AS INHIBITORS OF CYCLOOXYGENASE-2
-
Page 29, (2010/02/07)
The invention encompasses the novel comp...
The absolute configuration of cuauhtemone and related compounds
Torres-Valencia, J. Martin,Quintero-Mogica, Dora L.,Leon, Guadalupe I.,Suarez-Castillo, Oscar R.,Villagomez-Ibarra, J. Roberto,Maldonado, Emma,Cerda-Garcia-Rojas, Carlos M.,Joseph-Nathan, Pedro
, p. 543 - 548 (2007/10/03)
The absolute configuration of cuauhtemon...
41051-72-3 Process route
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-
563-46-2
2-Methyl-1-butene
-
-
41051-72-3
2-methyl-1,2-butanediol
| Conditions | Yield |
|---|---|
|
2-Methyl-1-butene;
With
Oxone; sodium chloride;
In
water; acetone;
at 650 ℃;
for 20h;
Large scale;
With
water; sodium hydroxide;
at 25 - 60 ℃;
for 7h;
pH=12;
Large scale;
|
82% |
|
With
peracetic acid;
und Verseifen des entstandenen Oels;
|
|
|
With
potassium permanganate;
|
|
|
With
osmium(VIII) oxide; dihydrogen peroxide; tert-butyl alcohol;
at 0 ℃;
|
|
|
With
osmium(VIII) oxide; dihydrogen peroxide; tert-butyl alcohol;
at 0 ℃;
|
-
-
925-90-6
ethylmagnesium bromide
-
-
116-09-6
hydroxy-2-propanone
-
-
41051-72-3
2-methyl-1,2-butanediol
| Conditions | Yield |
|---|---|
|
In
diethyl ether;
at 0 - 20 ℃;
for 0.5h;
|
41051-72-3 Upstream products
-
186581-53-3
diazomethane
-
78-93-3
butanone
-
30095-63-7
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-
6656-60-6
2-oxopropyl benzoate
41051-72-3 Downstream products
-
96-17-3
2-Methylbutyraldehyde
-
23378-11-2
1-chloro-2-methyl-but-1-ene
-
88476-29-3
1-<(p-tolylsulfonyl)oxy>-2-methyl-2-butyl phenylcarbamate
-
1354575-70-4
C13H18O3
