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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide

(R)-(+)-4-METHOXYMANDELONITRILE synthesis

7synthesis methods
HYDROGEN CYANIDE

74-90-8
4 suppliers
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123-11-5 Synthesis
p-Anisaldehyde

123-11-5
842 suppliers
$10.00/10g

(R)-(+)-4-METHOXYMANDELONITRILE

97070-73-0
15 suppliers
$67.20/1G

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Yield:97070-73-0 100%

Reaction Conditions:

with almond meal;citrate buffer pH 5.5 in ethyl acetate at 4;

References:

Zandbergen;Van der Linden;Brussee;Van der Gen [Synthetic Communications,1991,vol. 21,# 12-13,p. 1387 - 1391]

Benzeneacetonitrile, 4-methoxy-α-[(trimethylsilyl)oxy]-, (αR)-

120390-74-1
0 suppliers
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(R)-(+)-4-METHOXYMANDELONITRILE

97070-73-0
15 suppliers
$67.20/1G

References
7677-24-9 Synthesis
Trimethylsilyl cyanide

7677-24-9
374 suppliers
$19.00/5g

123-11-5 Synthesis
p-Anisaldehyde

123-11-5
842 suppliers
$10.00/10g

(R)-(+)-4-METHOXYMANDELONITRILE

97070-73-0
15 suppliers
$67.20/1G

References
POTASSIUM CYANIDE

151-50-8
4 suppliers
$47.79/100g

123-11-5 Synthesis
p-Anisaldehyde

123-11-5
842 suppliers
$10.00/10g

(R)-(+)-4-METHOXYMANDELONITRILE

97070-73-0
15 suppliers
$67.20/1G

References
773837-37-9 Synthesis
sodium:cyanide

773837-37-9
0 suppliers
inquiry

123-11-5 Synthesis
p-Anisaldehyde

123-11-5
842 suppliers
$10.00/10g

(R)-(+)-4-METHOXYMANDELONITRILE

97070-73-0
15 suppliers
$67.20/1G

References

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