BENZYL L-LACTATE

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Names

[ CAS No. ]:
56777-24-3

[ Name ]:
BENZYL L-LACTATE

[Synonym ]:
MFCD00209546
BenzylL-lactate
L-benzyl lactate
N-BENZYLLACTATE
l-lactic acid benzyl ester

Chemical & Physical Properties

[ Density]:
1.12 g/mL at 25 °C(lit.)

[ Boiling Point ]:
105-109 °C0.1 mm Hg(lit.)

[ Melting Point ]:
17 °C

[ Molecular Formula ]:
C10H12O3

[ Molecular Weight ]:
180.20000

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
180.07900

[ PSA ]:
46.53000

[ LogP ]:
1.11060

[ Index of Refraction ]:
n20/D 1.511(lit.)

[ Storage condition ]:
Refrigerator

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Safety Phrases ]:
S23-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2918110000

Synthetic Route

Precursor & DownStream

Precursor

  • L-Lactic acid
  • Benzyl bromide
  • Diphenylacetic Anhydride
  • Benzyl 2-hydroxypropanoate
  • 2,2-Diphenylacetic acid
  • Benzoic anhydride
  • Benzoic acid,4-methoxy-, 1,1'-anhydride
  • (3R,6R)-3,6-dimethyl-1,4-dioxane-2,5-dione
  • Benzyl alcohol

DownStream

Customs

[ HS Code ]: 2918110000

[ Summary ]:
2918110000. lactic acid, its salts and esters. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

Articles

Stereospecific Inhibitory Effects of CCG-1423 on the Cellular Events Mediated by Myocardin-Related Transcription Factor A.

PLoS ONE 10 , e0136242, (2015)

CCG-1423 suppresses several pathological processes including cancer cell migration, tissue fibrosis, and the development of atherosclerotic lesions. These suppressions are caused by inhibition of myoc...


More Articles


Related Compounds

  • Benzyl L-α-asparaginate
  • Benzyl L-leucinate hydrochloride (1:1)
  • Benzyl L-homoserinate
  • benzyl L-histidinate dihydrochloride
  • Benzyl L-valyl-L-prolinate hydrochloride
  • Benzyl-L-carbylhistidinmethylester
  • benzyl N-[(6-bromo-2,2-dimethyl-1,3-dioxaindan-5-yl)methyl]carbamate
  • tert-butyl (3R,4S)-4-[2-(tert-butoxy)-2-oxoethyl]-3-ethenylpiperidine-1-carboxylate
  • 3-[3-(acetamidomethyl)phenyl]-1H-1,2,4-triazole-5-carboxylic acid
  • rac-(3R,4R)-1-acetyl-3-methylpiperidine-4-carboxylic acid
  • 2-cyclopropyl-5-acetamido-1H-imidazole-4-carboxylic acid
  • Methyl 3-(morpholin-2-yl)-1,2-oxazole-5-carboxylate
  • 2-(N-ethyl-2,2,2-trifluoroacetamido)-4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acid
  • benzyl N-[(4-bromo-1H-pyrrol-2-yl)methyl]carbamate
  • benzyl N-(2-{[(6-chloropyridin-3-yl)methyl]sulfanyl}ethyl)carbamate
  • 1-Acetyl-4-methoxypiperidine-3-carboxylic acid
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