主要文件

查看所有文档

S7602

丁香醛

Name: 丁香醛
Brand: ALDRICH

98%

别名:

3,5-二甲氧基-4-羟基苯甲醛, 4-羟基-3,5-二甲氧基苯甲醛

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:

HOC₆H₂(OCH₃)₂CHO

化学文摘社编号:

134-96-3

分子量:

182.17

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24899757

EC Number:

205-167-5

Beilstein/REAXYS Number:

784514

MDL number:

MFCD00006943

Assay:

98%

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

Quality Level

100

assay

98%

bp

192-193 °C/14 mmHg (lit.)

mp

110-113 °C (lit.)

SMILES string

COc1cc(C=O)cc(OC)c1O

InChI

1S/C9H10O4/c1-12-7-3-6(5-10)4-8(13-2)9(7)11/h3-5,11H,1-2H3

InChI key

KCDXJAYRVLXPFO-UHFFFAOYSA-N

说明

Still not finding the right product?

Explore all of our products under 丁香醛

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

Inhibitory action of toxic compounds present in lignocellulosic hydrolysates on xylose to xylitol bioconversion by Candida guilliermondii.

Rogério S Pereira et al.

Journal of industrial microbiology & biotechnology, 38(1), 71-78 (2010-09-08)

The inhibitory action of acetic acid, ferulic acid, and syringaldehyde on metabolism of Candida guilliermondii yeast during xylose to xylitol bioconversion was evaluated. Assays were performed in buffered and nonbuffered semidefined medium containing xylose as main sugar (80.0 g/l), supplemented

Effects of biomass hydrolysis by-products on oleaginous yeast Rhodosporidium toruloides.

Cuimin Hu et al.

Bioresource technology, 100(20), 4843-4847 (2009-06-06)

Lignocellulosic biomass hydrolysis inevitably coproduces byproducts that may have various affects on downstream biotransformation. It is imperative to document the inhibitor tolerance ability of microbial strain in order to utilize biomass hydrolysate more effectively. To achieve better lipid production by

Mechanism inspired development of rationally designed dihydrofolate reductase inhibitors as anticancer agents.

Palwinder Singh et al.

Journal of medicinal chemistry, 55(14), 6381-6390 (2012-06-28)

On the basis of structural analysis of dihydrofolate reductase (DHFR) (cocrystallized separately with NADPH, dihydrofolate and NADPH, trimethoprim), compounds 2 and 3 were optimized for inhibition of DHFR. Appreciable tumor growth inhibitory activities of compounds 2 and 3 over 60

查看所有相关文献

全球贸易项目编号

货号	GTIN
S7602-2G	04061832491172
S7602-5G	04061835282999
S7602-100G	04061832491158
S7602-25G	04061836960124