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4-Hydroxy-3-hydroxymethyl-3-methyl-2-butanone, also known as 4-hydroxy-3-(hydroxymethyl)-3-methyl-2-butanone, is an organic compound with the molecular formula C6H12O3. It is a colorless liquid with a molecular weight of 132.16 g/mol. 4-Hydroxy-3-hydroxymethyl-3-methyl-2-butanone is characterized by the presence of a hydroxyl group (-OH) at the 4-position, a hydroxymethyl group (-CH2OH) at the 3-position, and a methyl group (-CH3) at the 3-position as well. It is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure, it exhibits various chemical properties, such as reactivity towards nucleophiles and electrophiles, making it a versatile building block in organic synthesis.

6868-97-9

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6868-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6868-97-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,6 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6868-97:
(6*6)+(5*8)+(4*6)+(3*8)+(2*9)+(1*7)=149
149 % 10 = 9
So 6868-97-9 is a valid CAS Registry Number.

6868-97-9SDS

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 4-hydroxy-3-(hydroxymethyl)-3-methylbutan-2-one

1.2 Other means of identification

Product number -
Other names 4-hydroxy-3-hydroxymethyl-3-methyl-butan-2-one

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:6868-97-9 SDS

6868-97-9Relevant academic research and scientific papers

Synthesis of dInaphtho[2,1-d, g][1,3] dioxocin derivatives from α,α-bishydroxymethyl-2-butanone

Kumbaraci, Volkan,Karliga, Bekir,Kumbaraci, Ash,Akar, Ahmet,Talinli, Naciye

, p. 603 - 606 (2007/10/03)

Ketoaldehydes which are formed in situ by the rearrangement of α,aα-Bishydroxymethyl-2-butanone in acidic medium, reacted with 2-naphthol. New dinaphtho[2,1-d,g][1,3] dioxocin derivatives were synthesized.

SYNTHESIS OF 5-ALKENYL-1,3-DIOXANES

Lesnikova, E. T.,Zlotskii, S. S.,Rakhmankulov, D. L.

, p. 30 - 32 (2007/10/02)

Cyclic acetals containing alkenyl groups were obtained from 5-methyl-5-acetyl-1,3-dioxane.The 1,3-dioxane fragment does not interfere in reduction of the carbonyl group, nor in participation of the carbonyl group in Wittig and Grignard reactions.

Combatting fungi with 1-(azol-1-yl)-4-halo-(1)-phenoxy-butan-2-ones and -ols

-

, (2008/06/13)

Fungicidal 1-(azol-1-yl)-4-halo-1-phenoxy-butan-2-ones and -ols of the formula STR1 in which R represents alkyl with 1 to 4 carbon atoms; X represents hydrogen, alkyl with 1 to 4 carbon atoms or halogen; Y represents halogen; Z represents halogen, straignt-chain or branched alkyl with 1 to 4 carbon atoms, cycloalkyl with 5 to 7 carbon atoms, halogenoalkyl with 1 or 2 carbon atoms and 1 to 5 halogen atoms, alkoxy with one or 2 carbon atoms, alkylthio with 1 or 2 carbon atoms, alkoxycarbonyl with 1 to 5 carbon atoms in the alkoxy part, amino, cyano, nitro, phenyl or phenoxy substituted with at least one of halogen, amino, cyano, nitro and alkyl with 1 to 2 carbon atoms, phenylalkyl with 1 or 2 carbon atoms on the alkyl part optionally substituted in the alkyl part by alkylcarbonyl with a total of up to 3 carbon atoms and in the phenyl part by halogen, nitro or cyano; n represents 0,1,2 or 3, A is --CO-- or CH(OH)--, and B is --N= or --CH=, or a salt thereof.

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