56553-60-7

  • Product Name:Sodium triacetoxyborohydride
  • Molecular Formula:C6H10BNaO6
  • Purity:99%
  • Molecular Weight:211.943
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Product Details

pd_meltingpoint:116-120 °C (dec.)(lit.)

Appearance:white crystalline powder

Purity:99%

Quality products make an important contribution to long-term revenue and profitability. Quality Factory Sells Top Purity 99% Sodium triacetoxyborohydride 56553-60-7 with Safe Delivery

1.What is the Sodium triacetoxyborohydride ?

Sodium Triacetoxyborohydride(STAB) is a hydride reagent used in stereoselective reductive amination. It is able to replace toxic sodium cyanoborohydride under most conditions. It is selective in reducing aldehydes to alcohols in the presence of ketones. STAB is also stable in anhydrous acids, which enables reductive amination of aldehydes and ketones. It used in reductive amination of ketones and aldehydes and reductive amination/lactamization of carbonyl compounds with amines. The advantage of STAB compared to sodium cyanoborohydride is evident. STAB, being non-toxic, is easier to handle and forms no toxic by-products, making the treatment of process waste after the reaction simple and less costly.

acetic acid
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acetic acid

sodium tris(acetoxy)borohydride
56553-60-7

sodium tris(acetoxy)borohydride

Conditions
Conditions Yield
With sodium tetrahydroborate; In benzene;
With sodium tetrahydroborate; at 15 - 20 ℃;
With sodium tetrahydroborate; In 2-methylpropyl acetate; at 0 - 5 ℃; for 1h;
With sodium tetrahydroborate; In dichloromethane; for 2h;
With sodium tetrahydroborate; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere; Schlenk technique;
sodium tetrahydroborate
16940-66-2

sodium tetrahydroborate

sodium tris(acetoxy)borohydride
56553-60-7

sodium tris(acetoxy)borohydride

Conditions
Conditions Yield
With acetic acid; In benzene; byproducts: H2; under N2-atmosphere; slurry of NaBH4 in benzene cooled (10°C); CH3COOH added dropwise (temp. < 20°C); mixt. warmed (ambient temp.) and stirred for 8h;; filtration; white powder washed (ether) and held under vacuum over night; elem. anal.;;
92%

2.What is the CAS number for Sodium triacetoxyborohydride ?

The CAS number of Sodium triacetoxyborohydride is 56553-60-7.

More information of Sodium triacetoxyborohydride 56553-60-7 are:

CAS Number

56553-60-7

Density

1.36[at 20℃]

Melting Point

116-120 °C (dec.)(lit.)

Boiling Point

111.1℃[at 101 325 Pa]

Vapor Pressure

0Pa at 25℃

HS CODE

2850.00

PSA

78.90000

LogP

-0.60710

3.What are another words for Sodium triacetoxyborohydride ?

Synonyms for Sodium triacetoxyborohydride 56553-60-7:Sodium Triacetoxyborohydride (STAB);Sodium triacetoxyborohyride;Sodium triacetoborohydride;Sodium Triacetoxysborobydride;

4.What is the molecular formula of Sodium triacetoxyborohydride?

The chemical formula of  Sodium triacetoxyborohydride is C6H10BNaO6 which containing 6 Carbon atoms,10 Hydrogen atoms,1 Boron atoms,1 Sodium atoms and 6 Oxygen atoms,and the molecular weight of  Sodium triacetoxyborohydride is 211.943.

5.What is Sodium triacetoxyborohydride (56553-60-7) used for?

Sodium triacetoxyborohydride (STAB) is a hydride reagent known for its role in stereoselective reductive amination. It is a non-toxic alternative to the toxic sodium cyanoborohydride and is selective in reducing aldehydes to alcohols in the presence of ketones. STAB's stability in anhydrous acids allows for the reductive amination of aldehydes and ketones.

InChI:InChI=1/C6H10BO6.Na/c1-11-4(8)7(5(9)12-2)6(10)13-3;/h7H,1-3H3;/q-1;+1/rC6H10BNaO6/c1-12-4(9)7(8,5(10)13-2)6(11)14-3/h7H,1-3H3

Relevant articles related to Sodium triacetoxyborohydride:

Article

Source

Synthesis from (+)-α-pinene of optically active macrocycles containing cyclobutane, ester, azine, or hydrazide groups

Ishmuratov,Mingaleeva,Shakhanova,Muslukhov,Yakovleva,Botsman,Tolstikov

, p. 210 - 214 (2011)

Two-step stereocontrolled synthesis of densely functionalized cyclic β-aminoesters containing four stereocenters, based on a new cerium(IV) ammonium nitrate catalyzed sequential three-component reaction

Sridharan, Vellaisamy,Menendez, J. Carlos

, p. 4303 - 4306 (2008)

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