CAS 40348-66-1

(2R)-1,2-Butanediol

Formula: C₄H₁₀O₂

InChI: InChI=1S/C4H10O2/c1-2-4(6)3-5/h4-6H,2-3H2,1H3/t4-/m1/s1

InChI key: InChIKey=BMRWNKZVCUKKSR-SCSAIBSYSA-N

SMILES: [C@@H](CC)(CO)O

Synonyms:

• (-)-1,2-Butanediol
• (2R)-1,2-Butanediol
• (2R)-Butane-1,2-diol
• 1,2-Butanediol, (R)-
• 1,2-butanediol, (2R)-
• (R)-(-)-1,2-Butanediol

(R)-1,2-Butanediol

CAS: 40348-66-1

Formula: C₄H₁₀O₂

Purity: >98.0%(GC)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 90.12

Ref: 3B-B4118

(R)-Butane-1,2-diol

CAS: 40348-66-1

Formula: C₄H₁₀O₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 90.1210

Ref: IN-DA00I7WU

(2R)-Butane-1,2-diol

CAS: 40348-66-1

(2R)-Butane-1,2-diol

Formula: C₄H₁₀O₂

Purity: >98%

Color and Shape: Pale yellow Liquid

Molecular weight: 90.121

Ref: 54-OR52088

(R)-Butane-1,2-diol

CAS: 40348-66-1

Formula: C₄H₁₀O₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 90.122

Ref: 10-F238432

(R)-Butane-1,2-diol

CAS: 40348-66-1

(R)-Butane-1,2-diol

Formula: C₄H₁₀O₂

Purity: 98%

Molecular weight: 90.12

Ref: IN-DG46996

(R)-1,2-Butanediol

CAS: 40348-66-1

(R)-1,2-Butanediol is a chemical compound that is classified as a diol. It has two hydroxyl groups and is an active substance. The (R)-1,2-Butanediol molecule consists of two asymmetric carbon atoms. In the presence of oxygen, it can form a ternary complex with copper and the hydroxyl group. This ternary complex catalyzes the conversion of various substrates such as L-xylulose to its corresponding ketones or L-arabinose to its corresponding acetals. The reaction proceeds via substrate binding to the active site on the ternary complex and subsequent functional group participation in the reaction.

Formula: C₄H₁₀O₂

Purity: Min. 95%

Molecular weight: 90.12 g/mol

Ref: 3D-FB60197