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135357-96-9

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135357-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135357-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,3,5 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135357-96:
(8*1)+(7*3)+(6*5)+(5*3)+(4*5)+(3*7)+(2*9)+(1*6)=139
139 % 10 = 9
So 135357-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H31NO4/c1-5-6-7-8-9-10-11-14(2)18-19(24-16(21)12-20)17(22-4)15(3)13-23-18/h7-11,15,17-19H,5-6,12-13,20H2,1-4H3/b8-7+,10-9+,14-11+/t15-,17-,18+,19+/m1/s1

135357-96-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S,3S,4R,5R)-2-[(2E,4E,6E)-deca-2,4,6-trien-2-yl]-4-methoxy-5-methyloxan-3-yl] 2-aminoacetate

1.2 Other means of identification

Product number -
Other names Glycine,tetrahydro-4-methoxy-5-methyl-2-(1-methyl-1,3,5-nonatrienyl)-2H-pyran-3-yl ester,(2S-(2alpha(1E,3E,5E),3beta,4alpha,5alpha))

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:135357-96-9 SDS

135357-96-9Downstream Products

135357-96-9Relevant academic research and scientific papers

Targeted Genome Mining Reveals the Biosynthetic Gene Clusters of Natural Product CYP51 Inhibitors

Liu, Nicholas,Abramyan, Elizabeth D.,Cheng, Wei,Perlatti, Bruno,Harvey, Colin J.B.,Bills, Gerald F.,Tang, Yi

, p. 6043 - 6047 (2021)

Lanosterol 14α-demethylase (CYP51) is an important target in the development of antifungal drugs. The fungal-derived restricticin 1 and related molecules are the only examples of natural products that inhibit CYP51. Here, using colocalizations of genes en

Anti aldol reactions of α-alkoxymethyl ketones: Application to the total synthesis of (+)-restricticin

Paterson, Ian,Nowak, Thorsten

, p. 8243 - 8246 (2007/10/03)

The antifungal agent (+)-restricticin (1) was prepared in 12 steps from ketone (S)-8. The key steps are (i) the boron-mediated anti aldol reaction of (S)-8 with 9 to give 13 and (ii) the cyclisation reaction 4 → 15.

Total synthesis of restricticin

Jendrzejewski, Stefan,Ermann, Peter

, p. 615 - 618 (2007/10/02)

The novel antifungal antibiotic restriction was synthesized from L-mannose.

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