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(2R,3R)-2,3-Diaminobutane-1,4-diol is a chemical compound characterized by the presence of two primary amine groups and two hydroxyl groups. It is a versatile building block used in the synthesis of various pharmaceuticals, organic compounds, and serves as a valuable reagent in chemical research and development. (2R,3R)-2,3-DIAMINOBUTANE-1,4-DIOL is known for its unique structure and reactivity, which contribute to its wide range of applications in medicine, biochemistry, and material science.

136598-06-6

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136598-06-6 Usage

Uses

Used in Pharmaceutical Synthesis:
(2R,3R)-2,3-Diaminobutane-1,4-diol is utilized as a key intermediate in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs and therapeutic agents. Its presence in the molecular structure allows for the creation of complex molecules with potential medicinal properties.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, (2R,3R)-2,3-Diaminobutane-1,4-diol is employed as a starting material for the synthesis of various organic compounds. Its reactivity and functional groups enable the formation of diverse chemical entities with different applications.
Used in Chemical Research and Development:
(2R,3R)-2,3-Diaminobutane-1,4-diol serves as an important reagent in chemical research and development, where it is used to study the properties and reactions of various chemical systems. Its unique structure allows researchers to explore new pathways and mechanisms in chemical reactions.
Used in Material Science:
In the realm of material science, (2R,3R)-2,3-Diaminobutane-1,4-diol is used as a building block for the creation of new materials with specific properties. Its versatility in forming covalent bonds and interactions with other molecules makes it suitable for the development of advanced materials with applications in various industries.
Overall, (2R,3R)-2,3-Diaminobutane-1,4-diol is a multifaceted chemical compound with a broad spectrum of applications across different fields, making it an indispensable component in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 136598-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,9 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136598-06:
(8*1)+(7*3)+(6*6)+(5*5)+(4*9)+(3*8)+(2*0)+(1*6)=156
156 % 10 = 6
So 136598-06-6 is a valid CAS Registry Number.

136598-06-6Downstream Products

136598-06-6Relevant articles and documents

Efficient synthesis of (2R,3R)- and (2S,3S)-2,3-diaminobutane-1,4-diol and their dibenzyl ethers

Scheurer, Andreas,Mosset, Paul,Saalfrank, Rolf W.

, p. 1243 - 1251 (2007/10/03)

(2R,3R)-2,3-Diaminobutane-1,4-diol 6 and its dibenzyl ether 7 were efficiently synthesized starting from L-tartaric acid 1a. The crucial step, debenzylation of intermediate dibenzyloxydiazide 4, was accomplished in good yield by boron trichloride-dimethyl sulfide complex. The enantiomeric series was similarly obtained starting from D-tartaric acid.

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